A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505111



Internal ID20878377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76535854..76550369hg38UCSC Ensembl
chr15:76828195..76842710hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3814516
hg1914516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025785
Samples
Known GenesSCAPER
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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