A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520212



Internal ID15100819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4354619..4390827hg38UCSC Ensembl
Innerchr16:4404620..4440828hg19UCSC Ensembl
Innerchr16:4344621..4380829hg18UCSC Ensembl
Innerchr16:4344621..4380829hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3836209
hg1936209
hg1836209
hg1736209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663724, nssv698754, nssv661903
Samples
Known GenesCORO7, CORO7-PAM16, VASN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520212
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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