A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019396



Internal ID22081027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177046312..177218355hg38UCSC Ensembl
Outerchr4:177045394..177220157hg38UCSC Ensembl
Innerchr4:177967466..178139509hg19UCSC Ensembl
Outerchr4:177966548..178141311hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38174764
hg19174764
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156273
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4019396
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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