A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037967



Internal ID19127186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74104187..74131604hg38UCSC Ensembl
Innerchr14:74570890..74598307hg19UCSC Ensembl
Innerchr14:73640643..73668060hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3827418
hg1927418
hg1827418
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1939n100
Supporting Variantsnssv3531182, nssv3531183
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)nsv1037967
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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