A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368677



Internal ID21026230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35932304..35933088hg38UCSC Ensembl
chr4:35933926..35934710hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368677
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