A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234816



Internal ID20801856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64432101..64470200hg38UCSC Ensembl
chr9:69444519..69482618hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3838100
hg1938100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234816
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00195


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