A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519184



Internal ID15446477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:55927181..55936769hg38UCSC Ensembl
Innerchr2:56154316..56163904hg19UCSC Ensembl
Innerchr2:56007820..56017408hg18UCSC Ensembl
Innerchr2:56065967..56075555hg17UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg389589
hg199589
hg189589
hg179589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696668
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519184
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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