A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156871



Internal ID15878103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:122170717..122658757hg38UCSC Ensembl
Innerchr8:123182956..123670996hg19UCSC Ensembl
Innerchr8:123252137..123740177hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38488041
hg19488041
hg18488041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612136
Supporting Variants
SamplesHGDP01095
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156871
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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