A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623786



Internal ID7010642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71951580..71961784hg38UCSC Ensembl
Innerchr10:71951730..71961634hg38UCSC Ensembl
Outerchr10:71951430..71961934hg38UCSC Ensembl
chr10:73711338..73721542hg19UCSC Ensembl
Innerchr10:73711488..73721392hg19UCSC Ensembl
Outerchr10:73711188..73721692hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3810205
hg1910205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861549, essv13861548
SamplesNA19917, NA19372
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623786
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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