A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947496



Internal ID32366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1866787..1866843hg38UCSC Ensembl
chr4:1868514..1868570hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947496
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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