A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499796



Internal ID276754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110025269..110037941hg38UCSC Ensembl
chr10:111785027..111797699hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3812673
hg1912673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041034
Samples
Known GenesADD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499796
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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