A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043765



Internal ID19132984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:33182514..33209026hg38UCSC Ensembl
Innerchr14:33651720..33678232hg19UCSC Ensembl
Innerchr14:32721471..32747983hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3826513
hg1926513
hg1826513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1864n100
Supporting Variantsnssv3528593, nssv3528592
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)nsv1043765
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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