A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434814



Internal ID21092367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13563701..13565000hg38UCSC Ensembl
chr9:13563700..13564999hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434814
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