A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv718338



Internal ID16012294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80055694..80091130hg38UCSC Ensembl
Innerchr1:80521379..80556815hg19UCSC Ensembl
Innerchr1:80293967..80329403hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3835437
hg1935437
hg1835437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546654
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)nssv718338
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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