A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150518



Internal ID15531251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8661290..8746097hg38UCSC Ensembl
Innerchr16:8755147..8839954hg19UCSC Ensembl
Innerchr16:8662648..8747455hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3884808
hg1984808
hg1884808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571409
Supporting Variants
SamplesHGDP01071
Known GenesABAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150518
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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