A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040685



Internal ID94832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116480758..116486200hg38UCSC Ensembl
chr10:118240270..118245712hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385443
hg195443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040685
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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