A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034450



Internal ID19123672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167887449..168071290hg38UCSC Ensembl
Innerchr4:168808600..168992441hg19UCSC Ensembl
Innerchr4:169045175..169229016hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38183842
hg19183842
hg18183842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5464n100
Supporting Variantsnssv3744506, nssv3635323, nssv3744500, nssv3744498, nssv3744499, nssv3635324, nssv3744503, nssv3744497, nssv3744501, nssv3744502, nssv3635320, nssv3744505, nssv3744504, nssv3635325, nssv3635321, nssv3635322
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034450
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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