A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462880



Internal ID240802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146548156..146554767hg38UCSC Ensembl
chr6:146869292..146875903hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg386612
hg196612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989618
Samples
Known GenesRAB32
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462880
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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