A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643617



Internal ID7030376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8405778..8410021hg38UCSC Ensembl
Innerchr19:8406278..8409521hg38UCSC Ensembl
Outerchr19:8404778..8411021hg38UCSC Ensembl
chr19:8470662..8474905hg19UCSC Ensembl
Innerchr19:8471162..8474405hg19UCSC Ensembl
Outerchr19:8469662..8475905hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384244
hg194244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15989205, essv15989213, essv15989158, essv15989193, essv15989165, essv15989157, essv15989196, essv15989211, essv15989197, essv15989195, essv15989189, essv15989164, essv15989204, essv15989170, essv15989179, essv15989183, essv15989210, essv15989166, essv15989215, essv15989191, essv15989223, essv15989163, essv15989160, essv15989167, essv15989182, essv15989178, essv15989175, essv15989219, essv15989173, essv15989199, essv15989153, essv15989172, essv15989200, essv15989208, essv15989207, essv15989162, essv15989156, essv15989217, essv15989201, essv15989222, essv15989186, essv15989218, essv15989203, essv15989212, essv15989169, essv15989214, essv15989171, essv15989188, essv15989221, essv15989192, essv15989198, essv15989180, essv15989206, essv15989161, essv15989176, essv15989209, essv15989187, essv15989155, essv15989184, essv15989216, essv15989174, essv15989190, essv15989154, essv15989220, essv15989181, essv15989185, essv15989194, essv15989202, essv15989177, essv15989159, essv15989168
SamplesNA19141, NA19222, HG03163, NA19399, NA18877, HG03115, HG03130, HG03521, HG03298, HG03190, NA19393, HG03193, NA20356, NA19107, HG03199, HG03133, NA19171, HG02621, NA19201, HG03135, HG03499, NA20317, HG03342, HG02922, HG02981, NA20340, NA19207, HG02420, NA19189, NA18520, HG02946, NA20355, HG03369, NA20318, NA19451, NA19210, HG03132, HG01882, NA18516, NA20126, HG02508, HG02757, HG02555, HG03311, HG03123, NA19118, NA18879, HG03476, HG01890, HG02586, NA19147, HG03117, HG03127, HG02814, HG03108, HG02771, NA19143, NA19117, NA20334, HG02107, HG02462, HG03351, NA19102, NA19096, NA19213, NA19121, HG02763, NA18511, NA18522, HG03118, NA19153
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643617
Frequency
Sample Size2504
Observed Gain0
Observed Loss71
Observed Complex0
Frequencyn/a


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