A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001009



Internal ID21910352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68459609..68464030hg38UCSC Ensembl
chr8:69371844..69376265hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg384422
hg194422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588508
Samples
Known GenesC8orf34
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001009
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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