A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444017



Internal ID21101570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129887405..129888371hg38UCSC Ensembl
chr9:132649684..132650650hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174660
Samples
Known GenesFNBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444017
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