A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395255



Internal ID21052808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42400462..42412294hg38UCSC Ensembl
chr4:42402479..42414311hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3811833
hg1911833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116411
Samples
Known GenesATP8A1, SHISA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395255
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