A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421013



Internal ID22478883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159532067..159613447hg38UCSC Ensembl
chr4:160453219..160534599hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3881381
hg1981381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898291
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421013
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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