A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506269



Internal ID20879547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23686801..23688300hg38UCSC Ensembl
chr15:23931948..23933447hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196830
Samples
Known GenesNDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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