A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632195



Internal ID7019005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56956447..56977944hg38UCSC Ensembl
chr13:57530581..57552078hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3821498
hg1921498
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14741444, essv14741446, essv14741445
SamplesHG01374, HG01572, HG01917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632195
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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