A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095688



Internal ID22004921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:54064270..54064270hg38UCSC Ensembl
chr10:55824030..55824030hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584933
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095688
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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