A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037522



Internal ID92771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72326405..72326425hg38UCSC Ensembl
chr10:74086163..74086183hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037522
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.059007


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