A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498334



Internal ID275326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122743940..122744765hg38UCSC Ensembl
chr10:124503456..124504281hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498334
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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