A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039375



Internal ID93972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120005155..120005206hg38UCSC Ensembl
chr10:121764667..121764718hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412227
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039375
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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