A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460302



Internal ID238292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36711789..36712024hg38UCSC Ensembl
chr6:36679566..36679801hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981365
Samples
Known GenesRAB44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460302
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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