A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002858



Internal ID18745390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35822..66815hg38UCSC Ensembl
Innerchr4:35822..66707hg19UCSC Ensembl
Innerchr4:25822..56707hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3830994
hg1930886
hg1830886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5067n100
Supporting Variantsnssv3738066, nssv3615265, nssv3615266, nssv3738067, nssv3738065
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002858
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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