A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449889



Internal ID21107442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130994446..130998465hg38UCSC Ensembl
chr9:133869833..133873852hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg384020
hg194020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176950
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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