A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013837



Internal ID21923180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94590987..94591160hg38UCSC Ensembl
chr8:95603215..95603388hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013837
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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