A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712296



Internal ID19010577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41376753..41535992hg38UCSC Ensembl
Innerchr14:41845956..42005195hg19UCSC Ensembl
Innerchr14:40915706..41074945hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38159240
hg19159240
hg18159240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043813
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)nssv3712296
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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