A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037361



Internal ID21946704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16888131..16888212hg38UCSC Ensembl
chr11:16909678..16909759hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584698
Samples
Known GenesPLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037361
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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