A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945733



Internal ID31159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3823002..3830049hg38UCSC Ensembl
chr4:3824729..3831776hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg387048
hg197048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945733
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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