A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035982



Internal ID21945325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31177975..31178369hg38UCSC Ensembl
chr11:31199522..31199916hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035982
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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