A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521337



Internal ID15101944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55510637..55585662hg38UCSC Ensembl
Innerchr16:55544549..55619574hg19UCSC Ensembl
Innerchr16:54102050..54177075hg18UCSC Ensembl
Innerchr16:54102050..54177075hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3875026
hg1975026
hg1875026
hg1775026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697945
Samples
Known GenesCAPNS2, LPCAT2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521337
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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