A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031537



Internal ID18774071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:58570390..58624412hg38UCSC Ensembl
Innerchr8:59482949..59536971hg19UCSC Ensembl
Innerchr8:59645503..59699525hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3854023
hg1954023
hg1854023
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689455
Samples
Known GenesNSMAF, SDCBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031537
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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