A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504835



Internal ID281629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110008857..110109038hg38UCSC Ensembl
chr10:111768615..111868796hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38100182
hg19100182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041033
Samples
Known GenesADD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504835
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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