A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040002



Internal ID21949345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40014850..40020300hg38UCSC Ensembl
chr11:40036400..40041850hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg385451
hg195451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040002
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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