A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183750



Internal ID20750790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91161909..91165021hg38UCSC Ensembl
chr9:93924191..93927303hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383113
hg193113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183750
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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