A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038525



Internal ID93416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75824062..75829677hg38UCSC Ensembl
chr10:77583820..77589435hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg385616
hg195616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480779
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038525
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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