A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654462



Internal ID18952743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:147842773..147875305hg38UCSC Ensembl
Innerchr6:148163909..148196441hg19UCSC Ensembl
Innerchr6:148205602..148238134hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3832533
hg1932533
hg1832533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028929
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3654462
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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