A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029532



Internal ID87379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4863625..4863651hg38UCSC Ensembl
chr10:4905817..4905843hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029532
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.088573


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