A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189191



Internal ID20756231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:964801..1047400hg38UCSC Ensembl
chr11:964801..1047400hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3882600
hg1982600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437790
Supporting Variants
Samples
Known GenesAP2A2, MUC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189191
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.60731


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