A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531190



Internal ID18829471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74104355..74131781hg38UCSC Ensembl
Innerchr14:74571058..74598484hg19UCSC Ensembl
Innerchr14:73640811..73668237hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3827427
hg1927427
hg1827427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039715
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)nssv3531190
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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