A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000021



Internal ID67596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73814266..73818032hg38UCSC Ensembl
chr7:73228596..73232362hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383767
hg193767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490528
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000021
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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