A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186181



Internal ID20753221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62831466..62852682hg38UCSC Ensembl
chr11:62598938..62620154hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3821217
hg1921217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464851
Supporting Variants
Samples
Known GenesSNHG1, STX5, WDR74
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00036


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