A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039170



Internal ID93851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113885170..113885172hg38UCSC Ensembl
chr10:115644929..115644931hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547766
Supporting Variants
Samples
Known GenesNHLRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039170
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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