A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv736020



Internal ID16029976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:207371962..207379937hg38UCSC Ensembl
Innerchr1:207545307..207553282hg19UCSC Ensembl
Innerchr1:205611930..205619905hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg387976
hg197976
hg187976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549085
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)nssv736020
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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