A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521351



Internal ID15448644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160809769..160839498hg38UCSC Ensembl
Innerchr6:161230801..161260530hg19UCSC Ensembl
Innerchr6:161150791..161180520hg18UCSC Ensembl
Innerchr6:161201212..161230941hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3829730
hg1929730
hg1829730
hg1729730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv398n21
Supporting Variantsnssv697962
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521351
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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