A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034707



Internal ID21944050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101505252..101505319hg38UCSC Ensembl
chr11:101375983..101376050hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593632
Samples
Known GenesTRPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034707
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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