A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039452



Internal ID94020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101232926..101240070hg38UCSC Ensembl
chr10:102992683..102999827hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg387145
hg197145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478505
Supporting Variants
Samples
Known GenesLBX1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039452
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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