A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012818



Internal ID21922161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56523938..56525256hg38UCSC Ensembl
chr8:57436497..57437815hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381319
hg191319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581454
Samples
Known GenesLINC00968
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012818
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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