A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500056



Internal ID20873281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23833829..23893342hg38UCSC Ensembl
chr15:24078976..24138489hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3859514
hg1959514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193995
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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