A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661903



Internal ID15051869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4354619..4386444hg38UCSC Ensembl
Innerchr16:4404620..4436445hg19UCSC Ensembl
Innerchr16:4344621..4376446hg18UCSC Ensembl
Innerchr16:4344621..4376446hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3831826
hg1931826
hg1831826
hg1731826
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520212
Supporting Variants
Samples
Known GenesCORO7, CORO7-PAM16, VASN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661903
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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