A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000041



Internal ID67607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93510687..93513647hg38UCSC Ensembl
chr7:93139999..93142959hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382961
hg192961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486046
Supporting Variants
Samples
Known GenesCALCR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000041
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001562


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