A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039873



Internal ID94304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101939624..101939675hg38UCSC Ensembl
chr10:103699381..103699432hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5409938
Supporting Variants
Samples
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039873
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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