A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508016



Internal ID20881313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60663677..60722479hg38UCSC Ensembl
chr15:60955876..61014678hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3858803
hg1958803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026047
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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