A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107471



Internal ID15960657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21854890..21906496hg38UCSC Ensembl
Innerchr8:21712401..21764007hg19UCSC Ensembl
Innerchr8:21768347..21819953hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3851607
hg1951607
hg1851607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610763
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)nssv1107471
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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