A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185948



Internal ID20752988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7359920..7369547hg38UCSC Ensembl
chr11:7381151..7390778hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg389628
hg199628
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452456
Supporting Variants
Samples
Known GenesSYT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185948
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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