A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081847



Internal ID21991080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35079618..35079618hg38UCSC Ensembl
chr15:35371819..35371819hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081847
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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