A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141051



Internal ID340246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2225405..2226828hg38UCSC Ensembl
chr5:2225519..2226942hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381424
hg191424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141051
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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