A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987279



Internal ID20554321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120768417..120775208hg38UCSC Ensembl
chr11:120639126..120645917hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg386792
hg196792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473548
Supporting Variants
Samples
Known GenesGRIK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987279
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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