A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610147



Internal ID16397556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8207524..8274909hg38UCSC Ensembl
Innerchr8:8065046..8132431hg19UCSC Ensembl
Innerchr8:8102456..8169841hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3867386
hg1967386
hg1867386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105875, nssv1105874
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610147
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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