A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611807



Internal ID16052530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:98093498..98127382hg38UCSC Ensembl
Innerchr8:99105726..99139610hg19UCSC Ensembl
Innerchr8:99174902..99208786hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3833885
hg1933885
hg1833885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156141
Samples1782681495_A
Known GenesC8orf47, HRSP12, POP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611807
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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