A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022580



Internal ID18765114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52759217..52801607hg38UCSC Ensembl
Innerchr6:52624015..52666405hg19UCSC Ensembl
Innerchr6:52731974..52774364hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3842391
hg1942391
hg1842391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5962n100
Supporting Variantsnssv3657468
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)nsv1022580
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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