A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033420



Internal ID89969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28588558..28588874hg38UCSC Ensembl
chr10:28877487..28877803hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490148
Supporting Variants
Samples
Known GenesWAC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033420
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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