A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234360



Internal ID20801401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11575214..11798377hg38UCSC Ensembl
chr9:11575214..11798377hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38223164
hg19223164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234360
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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