A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027144



Internal ID19116363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52767793..52808133hg38UCSC Ensembl
Innerchr6:52632591..52672931hg19UCSC Ensembl
Innerchr6:52740550..52780890hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3840341
hg1940341
hg1840341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5963n100
Supporting Variantsnssv3657473
Samples
Known GenesGSTA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027144
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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