A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156876



Internal ID15879007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:126213494..126265081hg38UCSC Ensembl
Innerchr8:127225738..127277326hg19UCSC Ensembl
Innerchr8:127294920..127346508hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3851588
hg1951589
hg1851589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612170
Supporting Variants
SamplesHGDP01290
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156876
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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