A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524504



Internal ID15451797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94834615..94964192hg38UCSC Ensembl
Innerchr6:95544333..95673909hg19UCSC Ensembl
Innerchr6:95601054..95730630hg18UCSC Ensembl
Innerchr6:95601054..95730630hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38129578
hg19129577
hg18129577
hg17129577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700448
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524504
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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