A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1122467



Internal ID15975653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136965092..137098799hg38UCSC Ensembl
Innerchr8:137977335..138111042hg19UCSC Ensembl
Innerchr8:138046517..138180224hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38133708
hg19133708
hg18133708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612488
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)nssv1122467
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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