A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624771



Internal ID7011621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122185324..122186636hg38UCSC Ensembl
Innerchr10:122185340..122186620hg38UCSC Ensembl
Outerchr10:122185308..122186652hg38UCSC Ensembl
chr10:123944839..123946151hg19UCSC Ensembl
Innerchr10:123944855..123946135hg19UCSC Ensembl
Outerchr10:123944823..123946167hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13953915, essv13953914, essv13953917, essv13953916
SamplesNA19076, HG01870, NA18559, NA18623
Known GenesTACC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624771
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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