A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609613



Internal ID6996534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76708316..76724976hg38UCSC Ensembl
chr6:77418033..77434693hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3816661
hg1916661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12435635, essv12435634, essv12435633
SamplesHG02521, HG00464, NA18546
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609613
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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