A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958687



Internal ID39765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156311906..156382692hg38UCSC Ensembl
chr4:157233058..157303844hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3870787
hg1970787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958687
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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