A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530211



Internal ID18828492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42496151..42655964hg38UCSC Ensembl
Innerchr14:42965354..43125167hg19UCSC Ensembl
Innerchr14:42035104..42194917hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38159814
hg19159814
hg18159814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042451
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)nssv3530211
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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