A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010594



Internal ID74691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37532116..37538069hg38UCSC Ensembl
chr8:37389634..37395587hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385954
hg195954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485894
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010594
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009525


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