A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524297



Internal ID15451590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:68316162..68321028hg38UCSC Ensembl
Innerchr2:68543294..68548160hg19UCSC Ensembl
Innerchr2:68396798..68401664hg18UCSC Ensembl
Innerchr2:68454945..68459811hg17UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg384867
hg194867
hg184867
hg174867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700198
Samples
Known GenesCNRIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524297
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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