A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654428



Internal ID18952709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140458389..140544857hg38UCSC Ensembl
Innerchr6:140779526..140865994hg19UCSC Ensembl
Innerchr6:140821219..140907687hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3886469
hg1986469
hg1886469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021431
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)nssv3654428
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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