A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677556



Internal ID15414208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35193311..35526596hg38UCSC Ensembl
Innerchr16:34427682..34760967hg19UCSC Ensembl
Innerchr16:34285183..34618468hg18UCSC Ensembl
Innerchr16:34285183..34618468hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38333286
hg19333286
hg18333286
hg17333286
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)nssv677556
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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