A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386317



Internal ID21043870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42498936..42499620hg38UCSC Ensembl
chr4:42500953..42501637hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38685
hg19685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116415
Samples
Known GenesATP8A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386317
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