A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv725201



Internal ID16019157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158757235..158759556hg38UCSC Ensembl
Innerchr1:158727025..158729346hg19UCSC Ensembl
Innerchr1:156993649..156995970hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382322
hg192322
hg182322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548005
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv725201
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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