A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504680



Internal ID20877943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90086467..90088951hg38UCSC Ensembl
chr15:90629699..90632183hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382485
hg192485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026927
Samples
Known GenesIDH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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