A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217916



Internal ID20784956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31592503..31659359hg38UCSC Ensembl
chr9:31592501..31659357hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3866857
hg1966857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217916
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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