A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038171



Internal ID93177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112725802..112726246hg38UCSC Ensembl
chr10:114485561..114486005hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512336
Supporting Variants
Samples
Known GenesVTI1A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038171
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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