A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185906



Internal ID20752946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77897507..77901754hg38UCSC Ensembl
chr11:77608553..77612800hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384248
hg194248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460371
Supporting Variants
Samples
Known GenesINTS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185906
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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