A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180328



Internal ID20747368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108529012..108762128hg38UCSC Ensembl
chr11:108399739..108632855hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38233117
hg19233117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461847
Supporting Variants
Samples
Known GenesDDX10, EXPH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180328
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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