A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499344



Internal ID276318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110144094..110146481hg38UCSC Ensembl
chr10:111903852..111906239hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382388
hg192388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499344
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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