A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636310



Internal ID6676419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44700959..44704263hg38UCSC Ensembl
Innerchr15:44700969..44704253hg38UCSC Ensembl
Outerchr15:44700949..44704273hg38UCSC Ensembl
chr15:44993157..44996461hg19UCSC Ensembl
Innerchr15:44993167..44996451hg19UCSC Ensembl
Outerchr15:44993147..44996471hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg383305
hg193305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233262, essv15233261, essv15233263, essv15233269, essv15233248, essv15233257, essv15233253, essv15233251, essv15233266, essv15233270, essv15233256, essv15233254, essv15233268, essv15233267, essv15233255, essv15233246, essv15233271, essv15233265, essv15233252, essv15233247, essv15233250, essv15233260, essv15233264, essv15233245, essv15233249, essv15233259, essv15233258
SamplesHG02574, HG03163, HG02852, HG02419, HG03521, HG03515, HG03199, HG02756, HG02922, HG01495, NA19207, HG01626, HG03343, HG03088, HG02582, HG03457, HG03428, NA18910, HG03027, NA19118, HG03382, HG02881, HG03451, NA19206, HG02667, HG03117, HG03072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636310
Frequency
Sample Size2504
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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