A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031993



Internal ID89036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32351862..32356432hg38UCSC Ensembl
chr10:32640790..32645360hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg384571
hg194571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482788
Supporting Variants
Samples
Known GenesEPC1, LOC102031319
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031993
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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