A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191942



Internal ID20758982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37474459..37479959hg38UCSC Ensembl
chr9:37474456..37479956hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg385501
hg195501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448811
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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