A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088117



Internal ID21997350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11467496..11467496hg38UCSC Ensembl
chr10:11509495..11509495hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591366
Samples
Known GenesUSP6NL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088117
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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