A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001137



Internal ID21910480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98161583..98161651hg38UCSC Ensembl
chr8:99173811..99173879hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001137
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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