A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011826



Internal ID21921169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141174080..141215417hg38UCSC Ensembl
chr5:140553661..140594989hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3841338
hg1941329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557235
Samples
Known GenesPCDHB10, PCDHB11, PCDHB12, PCDHB13, PCDHB16, PCDHB7, PCDHB8, PCDHB9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011826
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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