A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031966



Internal ID89019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30720337..30772894hg38UCSC Ensembl
chr10:31009266..31061823hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3852558
hg1952558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484933
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031966
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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