A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624586



Internal ID6664750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112588995..112619828hg38UCSC Ensembl
Innerchr10:112589011..112619813hg38UCSC Ensembl
Outerchr10:112588980..112619844hg38UCSC Ensembl
chr10:114348754..114379587hg19UCSC Ensembl
Innerchr10:114348770..114379572hg19UCSC Ensembl
Outerchr10:114348739..114379603hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3830834
hg1930834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv167e214
Supporting Variantsessv13939559, essv13939558
SamplesHG02318, HG03193
Known GenesVTI1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624586
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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