A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532198



Internal ID18830479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22139406..22501578hg38UCSC Ensembl
Innerchr14:22607365..22970562hg19UCSC Ensembl
Innerchr14:21677205..22040402hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38362173
hg19363198
hg18363198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036750
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)nssv3532198
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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