A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501139



Internal ID20874370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56884801..56890300hg38UCSC Ensembl
chr15:57176999..57182498hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179451
Samples
Known GenesLOC145783
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501139
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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