A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500847



Internal ID20874076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54506609..54507321hg38UCSC Ensembl
chr15:54798807..54799519hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025531
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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