A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657472



Internal ID18955753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52767793..52805646hg38UCSC Ensembl
Innerchr6:52632591..52670444hg19UCSC Ensembl
Innerchr6:52740550..52778403hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3837854
hg1937854
hg1837854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028837
Supporting Variants
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)nssv3657472
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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