A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv736992



Internal ID16030948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:218684355..218824090hg38UCSC Ensembl
Innerchr1:218857697..218997432hg19UCSC Ensembl
Innerchr1:216924320..217064055hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38139736
hg19139736
hg18139736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549219
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)nssv736992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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