A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369123



Internal ID21026676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2504719..2505533hg38UCSC Ensembl
chr4:2506446..2507260hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113383
Samples
Known GenesRNF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369123
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