A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510091



Internal ID20883406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56589933..56668676hg38UCSC Ensembl
chr15:56882131..56960874hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3878744
hg1978744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184272
Samples
Known GenesZNF280D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510091
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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