A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991443



Internal ID61710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2319888..2326516hg38UCSC Ensembl
chr7:2359523..2366151hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg386629
hg196629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470135
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991443
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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