A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531200



Internal ID18829481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74105984..74133932hg38UCSC Ensembl
Innerchr14:74572687..74600635hg19UCSC Ensembl
Innerchr14:73642440..73670388hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3827949
hg1927949
hg1827949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045729
Supporting Variants
Samples
Known GenesLIN52
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531200
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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