A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623161



Internal ID7010018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48989911..48999150hg38UCSC Ensembl
Innerchr10:48989911..48999150hg38UCSC Ensembl
Outerchr10:48989649..48999401hg38UCSC Ensembl
chr10:50197956..50207195hg19UCSC Ensembl
Innerchr10:50197956..50207195hg19UCSC Ensembl
Outerchr10:50197694..50207446hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg389240
hg199240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13796104, essv13796111, essv13796113, essv13796102, essv13796103, essv13796112, essv13796108, essv13796107, essv13796110, essv13796105, essv13796109, essv13796106
SamplesNA19141, HG03111, NA18504, HG03099, HG03499, HG02952, HG02922, NA19238, HG03511, NA19984, HG03129, HG03196
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623161
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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