A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502102



Internal ID20875343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98366711..98371493hg38UCSC Ensembl
chr15:98909940..98914722hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg384783
hg194783
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502102
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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