A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531169



Internal ID18829450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74101033..74132353hg38UCSC Ensembl
Innerchr14:74567736..74599056hg19UCSC Ensembl
Innerchr14:73637489..73668809hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3831321
hg1931321
hg1831321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051621
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)nssv3531169
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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