A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036256



Internal ID91916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59388840..59388891hg38UCSC Ensembl
chr10:61148598..61148649hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg386017
hg196017
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561117
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036256
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005339


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