A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041104



Internal ID95107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111148855..111150035hg38UCSC Ensembl
chr10:112908613..112909793hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041104
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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