A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521577



Internal ID15448870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166214601..166217703hg38UCSC Ensembl
Innerchr6:166628089..166631191hg19UCSC Ensembl
Innerchr6:166548079..166551181hg18UCSC Ensembl
Innerchr6:166598500..166601602hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383103
hg193103
hg183103
hg173103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698193
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521577
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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