A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039687



Internal ID94177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112024739..112024790hg38UCSC Ensembl
chr10:113784497..113784548hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5409343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039687
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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