A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511398



Internal ID20884725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43644701..43658600hg38UCSC Ensembl
chr15:43936899..43950798hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3813900
hg1913900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2513n223
Supporting Variantsnssv18185072
Samples
Known GenesCATSPER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511398
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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