A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1116987



Internal ID15970173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74452293..74460890hg38UCSC Ensembl
Innerchr8:75364528..75373125hg19UCSC Ensembl
Innerchr8:75527083..75535680hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg388598
hg198598
hg188598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611552
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)nssv1116987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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