A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520377



Internal ID15447670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103886804..104014680hg38UCSC Ensembl
Innerchr6:104334679..104462555hg19UCSC Ensembl
Innerchr6:104441372..104569248hg18UCSC Ensembl
Innerchr6:104441372..104569248hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38127877
hg19127877
hg18127877
hg17127877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693195, nssv695935, nssv663384
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520377
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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