A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042168



Internal ID19131387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:33186404..33207997hg38UCSC Ensembl
Innerchr14:33655610..33677203hg19UCSC Ensembl
Innerchr14:32725361..32746954hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3821594
hg1921594
hg1821594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1864n100
Supporting Variantsnssv3528595
Samples
Known GenesNPAS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042168
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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