A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015688



Internal ID22077319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152069134..152071589hg38UCSC Ensembl
Outerchr4:152068448..152072978hg38UCSC Ensembl
Innerchr4:152990286..152992741hg19UCSC Ensembl
Outerchr4:152989600..152994130hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg384531
hg194531
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156243
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015688
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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