A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511353



Internal ID20884680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51452057..51453391hg38UCSC Ensembl
chr15:51744254..51745588hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381335
hg191335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024017
Samples
Known GenesDMXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511353
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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