A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036634



Internal ID92168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96914319..96925222hg38UCSC Ensembl
chr10:98674076..98684979hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3810904
hg1910904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143457
Supporting Variants
Samples
Known GenesLCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036634
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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