A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444736



Internal ID21102289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124966351..124968263hg38UCSC Ensembl
chr9:127728630..127730542hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381913
hg191913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176640
Samples
Known GenesSCAI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444736
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