A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026838



Internal ID21936181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73709107..73715882hg38UCSC Ensembl
chr11:73420152..73426927hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386776
hg196776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586514
Samples
Known GenesRAB6A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026838
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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