A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176867



Internal ID20743907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128289401..128295000hg38UCSC Ensembl
chr9:131051680..131057279hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer