A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014543



Internal ID19103761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35374407..35403672hg38UCSC Ensembl
Innerchr4:35376029..35405294hg19UCSC Ensembl
Innerchr4:35052424..35081689hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3829266
hg1929266
hg1829266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5190n100
Supporting Variantsnssv3625006, nssv3625005, nssv3625004
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)nsv1014543
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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