A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503141



Internal ID279983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130262040..130351943hg38UCSC Ensembl
chr10:132060304..132150207hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3889904
hg1989904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503141
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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