A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654831



Internal ID18953112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22901391..23041148hg38UCSC Ensembl
Innerchr6:22901620..23041376hg19UCSC Ensembl
Innerchr6:23009599..23149355hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38139758
hg19139757
hg18139757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029070
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)nssv3654831
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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