A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030461



Internal ID88015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17882386..17882394hg38UCSC Ensembl
chr10:18171315..18171323hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538486
Supporting Variants
Samples
Known GenesMRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030461
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001873


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