A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993890



Internal ID63378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22416314..22421525hg38UCSC Ensembl
chr7:22455933..22461144hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385212
hg195212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458028
Supporting Variants
Samples
Known GenesSTEAP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993890
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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