A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv717751



Internal ID16011707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79666309..79888111hg38UCSC Ensembl
Innerchr1:80131994..80353796hg19UCSC Ensembl
Innerchr1:79904582..80126384hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38221803
hg19221803
hg18221803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546638
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)nssv717751
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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