A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174734



Internal ID20741774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16920472..16965340hg38UCSC Ensembl
chr9:16920470..16965338hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3844869
hg1944869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431565
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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