A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186751



Internal ID20753791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70401608..70402248hg38UCSC Ensembl
chr11:70247714..70248354hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472148
Supporting Variants
Samples
Known GenesCTTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186751
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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