A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036345



Internal ID21945688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83899681..83904955hg38UCSC Ensembl
chr11:83610724..83615998hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385275
hg195275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596151
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036345
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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