A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485934



Internal ID263313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28770633..28776166hg38UCSC Ensembl
chr10:29059562..29065095hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385534
hg195534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485934
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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