A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008160



Internal ID21917503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95567393..95589533hg38UCSC Ensembl
chr8:96579621..96601761hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3822141
hg1922141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583989
Samples
Known GenesLOC100616530
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008160
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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