A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177059



Internal ID20744099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132710946..132713920hg38UCSC Ensembl
chr9:135586333..135589307hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382975
hg192975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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