A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690775



Internal ID15427427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35234530..35532147hg38UCSC Ensembl
Innerchr16:34468901..34766518hg19UCSC Ensembl
Innerchr16:34326402..34624019hg18UCSC Ensembl
Innerchr16:34326402..34624019hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38297618
hg19297618
hg18297618
hg17297618
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)nssv690775
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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