A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172485



Internal ID20739525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108133701..108136600hg38UCSC Ensembl
chr9:110895981..110898880hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441593
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172485
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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