A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478826



Internal ID21136379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25504502..25508149hg38UCSC Ensembl
chr13:26078640..26082287hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg383648
hg193648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007472
Samples
Known GenesATP8A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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