A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192003



Internal ID20759043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120666463..120930716hg38UCSC Ensembl
chr11:120537172..120801425hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38264254
hg19264254
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456282
Supporting Variants
Samples
Known GenesGRIK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192003
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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