A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005849



Internal ID21915192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115960577..115960631hg38UCSC Ensembl
chr8:116972802..116972856hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579125
Samples
Known GenesLINC00536
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005849
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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