A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949714



Internal ID33813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43220073..43220305hg38UCSC Ensembl
chr4:43222090..43222322hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468121
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949714
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002966


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