A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522922



Internal ID15103529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102839465..103299084hg38UCSC Ensembl
Innerchr1:103305021..103764640hg19UCSC Ensembl
Innerchr1:103077609..103537228hg18UCSC Ensembl
Innerchr1:103017042..103476661hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38459620
hg19459620
hg18459620
hg17459620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698583
Samples
Known GenesCOL11A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522922
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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