A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184595



Internal ID20751635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3336264..3349891hg38UCSC Ensembl
chr18:3336262..3349889hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3813628
hg1913628
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524265
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184595
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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