A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040532



Internal ID94729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125613502..125715502hg38UCSC Ensembl
chr10:127302071..127404071hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38102001
hg19102001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512829
Supporting Variants
Samples
Known GenesFLJ37035, LOC283038, TEX36
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040532
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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