A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365438



Internal ID21022991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15948539..16088365hg38UCSC Ensembl
chr4:15950162..16089988hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38139827
hg19139827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111728
Samples
Known GenesFGFBP2, PROM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365438
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