A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485779



Internal ID263161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4222083..4225808hg38UCSC Ensembl
chr10:4264275..4268000hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383726
hg193726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029471
Samples
Known GenesLINC00702
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485779
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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