A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395132



Internal ID21052685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52794083..52794597hg38UCSC Ensembl
chr4:53660250..53660764hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117373
Samples
Known GenesLOC152578
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395132
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