A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617437



Internal ID7004322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63923367..63935483hg38UCSC Ensembl
chr8:64835924..64848040hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3812117
hg1912117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13213174, essv13213172, essv13213176, essv13213173, essv13213177, essv13213175
SamplesHG00351, NA18639, NA18642, HG01345, HG02497, NA19149
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617437
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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