A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992661



Internal ID20559701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60713885..60714299hg38UCSC Ensembl
chr11:60481358..60481772hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466781
Supporting Variants
Samples
Known GenesMS4A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01308


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