A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000487



Internal ID21909830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36795806..36798836hg38UCSC Ensembl
chr8:36653324..36656354hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383031
hg193031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569286
Samples
Known GenesKCNU1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000487
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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