A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156573



Internal ID15880842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8240557..8287918hg38UCSC Ensembl
Innerchr8:8098079..8145440hg19UCSC Ensembl
Innerchr8:8135489..8182850hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3847362
hg1947362
hg1847362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610150
Supporting Variants
SamplesNINDS_37
Known GenesFAM86B3P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156573
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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