A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512538



Internal ID20885873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43010901..43028900hg38UCSC Ensembl
chr15:43303099..43321098hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3818000
hg1918000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188568
Samples
Known GenesUBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512538
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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