A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008326



Internal ID21917669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92185157..92185238hg38UCSC Ensembl
chr6:92894875..92894956hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008326
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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