A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183500



Internal ID20750540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38372990..38442627hg38UCSC Ensembl
chr18:35952954..36022591hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3869638
hg1969638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183500
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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