A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735711



Internal ID159377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86174662..86234053hg38UCSC Ensembl
chr7:85803978..85863369hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3859392
hg1959392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735711
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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