A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460898



Internal ID238865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36802002..36802775hg38UCSC Ensembl
chr6:36769778..36770551hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38774
hg19774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981371
Samples
Known GenesCPNE5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460898
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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