A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018027



Internal ID18760560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52761471..52801607hg38UCSC Ensembl
Innerchr6:52626269..52666405hg19UCSC Ensembl
Innerchr6:52734228..52774364hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3840137
hg1940137
hg1840137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5962n100
Supporting Variantsnssv3657469
Samples
Known GenesGSTA1, GSTA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018027
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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