A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002590



Internal ID69344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128779749..128780505hg38UCSC Ensembl
chr7:128419803..128420559hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476279
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002590
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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