A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1105872



Internal ID15959058
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 StatusS
Merged Variantsnsv610146
Supporting Variants
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1105872
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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