A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039229



Internal ID19128448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74107460..74133932hg38UCSC Ensembl
Innerchr14:74574163..74600635hg19UCSC Ensembl
Innerchr14:73643916..73670388hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3826473
hg1926473
hg1826473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1939n100
Supporting Variantsnssv3531201
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)nsv1039229
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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