A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143402



Internal ID342603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103416285..103587640hg38UCSC Ensembl
chr11:103287013..103458368hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38171356
hg19171356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049550
Samples
Known GenesDYNC2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143402
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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