A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622557



Internal ID7009416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20499707..20529698hg38UCSC Ensembl
chr10:20788636..20818627hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3829992
hg1929992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv102e214
Supporting Variantsessv13713846, essv13713847, essv13713849, essv13713848
SamplesNA11829, HG01374, HG00246, NA20826
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622557
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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