A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178267



Internal ID20745307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102948543..102956665hg38UCSC Ensembl
chr11:102819272..102827394hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg388123
hg198123
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466302
Supporting Variants
Samples
Known GenesMMP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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