A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624757



Internal ID7011607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121674875..121703457hg38UCSC Ensembl
chr10:123434389..123462971hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3828583
hg1928583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv169e214
Supporting Variantsessv13953790, essv13953793, essv13953789, essv13953788, essv13953791, essv13953792
SamplesNA19448, NA12156, NA06984, HG01122, NA19982, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624757
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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