A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993873



Internal ID63366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22103323..22505243hg38UCSC Ensembl
chr7:22142941..22544862hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38401921
hg19401922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471102
Supporting Variants
Samples
Known GenesRAPGEF5, STEAP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993873
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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