A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391750



Internal ID21049303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34738040..34740666hg38UCSC Ensembl
chr5:34738145..34740771hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg382627
hg192627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129738
Samples
Known GenesRAI14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391750
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