A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711287



Internal ID16005243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:20230269..20278466hg38UCSC Ensembl
Innerchr1:20556762..20604959hg19UCSC Ensembl
Innerchr1:20429349..20477546hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3848198
hg1948198
hg1848198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545733
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)nssv711287
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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