A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449961



Internal ID21107514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132019651..132024274hg38UCSC Ensembl
chr9:134895038..134899661hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg384624
hg194624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177021
Samples
Known GenesMED27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449961
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