A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530994



Internal ID18829275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48286669..48478005hg38UCSC Ensembl
Innerchr14:48755872..48947208hg19UCSC Ensembl
Innerchr14:47825622..48016958hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38191337
hg19191337
hg18191337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035232
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)nssv3530994
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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