A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001924



Internal ID68887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81471146..81482796hg38UCSC Ensembl
chr7:81100462..81112112hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3811651
hg1911651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001924
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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