A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031969



Internal ID89021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31988255..31992357hg38UCSC Ensembl
chr10:32277183..32281285hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg384103
hg194103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474148
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031969
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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