A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156369



Internal ID15853191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73260207..73270322hg38UCSC Ensembl
Innerchr8:74172442..74182557hg19UCSC Ensembl
Innerchr8:74334996..74345111hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3810116
hg1910116
hg1810116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611539
Supporting Variants
Samples1780846005_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156369
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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