A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156567



Internal ID15874240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8236884..8287918hg38UCSC Ensembl
Innerchr8:8094406..8145440hg19UCSC Ensembl
Innerchr8:8131816..8182850hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3851035
hg1951035
hg1851035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610148
Supporting Variants
SamplesHGDP00512
Known GenesFAM86B3P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156567
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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