A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657474



Internal ID18955755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52771796..52808133hg38UCSC Ensembl
Innerchr6:52636594..52672931hg19UCSC Ensembl
Innerchr6:52744553..52780890hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3836338
hg1936338
hg1836338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033017
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)nssv3657474
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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