A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624764



Internal ID7011614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122028000..122030029hg38UCSC Ensembl
Innerchr10:122028013..122030017hg38UCSC Ensembl
Outerchr10:122027988..122030042hg38UCSC Ensembl
chr10:123787515..123789544hg19UCSC Ensembl
Innerchr10:123787528..123789532hg19UCSC Ensembl
Outerchr10:123787503..123789557hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382030
hg192030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13953888, essv13953890, essv13953885, essv13953887, essv13953886, essv13953889
SamplesHG02891, NA19190, NA18519, HG03394, NA19017, NA19475
Known GenesTACC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624764
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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