A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691960



Internal ID15428612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35193311..35571488hg38UCSC Ensembl
Innerchr16:34427682..34805859hg19UCSC Ensembl
Innerchr16:34285183..34663360hg18UCSC Ensembl
Innerchr16:34285183..34663360hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38378178
hg19378178
hg18378178
hg17378178
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516385
Supporting Variants
Samples
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691960
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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