A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382548



Internal ID21040101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40330085..40333686hg38UCSC Ensembl
chr4:40332102..40335703hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg383602
hg193602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117100
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382548
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