A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610146



Internal ID16397555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8185380..8287918hg38UCSC Ensembl
Innerchr8:8042902..8145440hg19UCSC Ensembl
Innerchr8:8080312..8182850hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38102539
hg19102539
hg18102539
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105872, nssv1105873
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610146
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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