A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519967



Internal ID15447260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102658247..102668353hg38UCSC Ensembl
Innerchr1:103123803..103133909hg19UCSC Ensembl
Innerchr1:102896391..102906497hg18UCSC Ensembl
Innerchr1:102835824..102845930hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3810107
hg1910107
hg1810107
hg1710107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694357
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519967
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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