A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194991



Internal ID20762031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132242760..132705630hg38UCSC Ensembl
chr11:132112654..132575525hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38462871
hg19462872
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474850
Supporting Variants
Samples
Known GenesNTM, NTM-IT, OPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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