A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011681



Internal ID21921024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11044386..11044451hg38UCSC Ensembl
chr6:11044619..11044684hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565483
Samples
Known GenesELOVL2, ELOVL2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011681
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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