A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504894



Internal ID20878158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66554143..66555372hg38UCSC Ensembl
chr15:66846481..66847710hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381230
hg191230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025421
Samples
Known GenesLCTL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504894
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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