A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1117717



Internal ID15624217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91110980..91161887hg38UCSC Ensembl
Innerchr8:92123208..92174115hg19UCSC Ensembl
Innerchr8:92192384..92243291hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3850908
hg1950908
hg1850908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611722
Supporting Variants
Samples
Known GenesLRRC69
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1117717
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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