A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998363



Internal ID66453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74156382..74156512hg38UCSC Ensembl
chr7:73570712..73570842hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487772
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998363
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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