A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486038



Internal ID21143591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25669698..25693808hg38UCSC Ensembl
chr13:26243836..26267946hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3824111
hg1924111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007464
Samples
Known GenesATP8A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer