A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037814



Internal ID18780345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73250066..73273941hg38UCSC Ensembl
Innerchr14:73716774..73740649hg19UCSC Ensembl
Innerchr14:72786527..72810402hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3823876
hg1923876
hg1823876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1934n100
Supporting Variantsnssv3531146, nssv3531149, nssv3531147, nssv3531148
Samples
Known GenesPAPLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037814
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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