A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144113



Internal ID343316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111156431..111242621hg38UCSC Ensembl
chr10:112916189..113002379hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3886191
hg1986191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144113
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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