A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036042



Internal ID91770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49159575..49159996hg38UCSC Ensembl
chr10:50367620..50368041hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475853
Supporting Variants
Samples
Known GenesC10orf128
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036042
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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