A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948123



Internal ID32778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40377005..40384115hg38UCSC Ensembl
chr4:40379022..40386132hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg387111
hg197111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472737
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948123
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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