A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001638



Internal ID18744169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43670..66815hg38UCSC Ensembl
Innerchr4:43671..66707hg19UCSC Ensembl
Innerchr4:33671..56707hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3823146
hg1923037
hg1823037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5068n100
Supporting Variantsnssv3615273
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)nsv1001638
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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