A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511616



Internal ID20884946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36602709..36620088hg38UCSC Ensembl
chr15:36894910..36912289hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3817380
hg1917380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185623
Samples
Known GenesC15orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511616
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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