A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148891



Internal ID15527666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1465161..1488362hg38UCSC Ensembl
Innerchr16:1515162..1538363hg19UCSC Ensembl
Innerchr16:1455163..1478364hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3823202
hg1923202
hg1823202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571162
Supporting Variants
SamplesHGDP00527
Known GenesCLCN7, PTX4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148891
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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