A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011049



Internal ID21920392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100425185..100425380hg38UCSC Ensembl
chr8:101437413..101437608hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011049
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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