A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031442



Internal ID88657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31751983..31755207hg38UCSC Ensembl
chr10:32040911..32044135hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383225
hg193225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491889
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031442
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002194


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