A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037821



Internal ID92958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120902679..120902730hg38UCSC Ensembl
chr10:122662191..122662242hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg385594
hg195594
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554904
Supporting Variants
Samples
Known GenesMIR5694, WDR11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037821
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.05702


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