A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682925



Internal ID15419577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35234530..35569018hg38UCSC Ensembl
Innerchr16:34468901..34803389hg19UCSC Ensembl
Innerchr16:34326402..34660890hg18UCSC Ensembl
Innerchr16:34326402..34660890hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38334489
hg19334489
hg18334489
hg17334489
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)nssv682925
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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