A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531167



Internal ID18829448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74101033..74131264hg38UCSC Ensembl
Innerchr14:74567736..74597967hg19UCSC Ensembl
Innerchr14:73637489..73667720hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3830232
hg1930232
hg1830232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050903
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)nssv3531167
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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