A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041034



Internal ID95065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110025269..110037941hg38UCSC Ensembl
chr10:111785027..111797699hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3812673
hg1912673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499796
Supporting Variants
Samples
Known GenesADD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041034
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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