A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521150



Internal ID15448443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:66385464..66439458hg38UCSC Ensembl
Innerchr1:66851147..66905141hg19UCSC Ensembl
Innerchr1:66623735..66677729hg18UCSC Ensembl
Innerchr1:66563168..66617162hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3853995
hg1953995
hg1853995
hg1753995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694421
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521150
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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