A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986229



Internal ID20553270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105876428..106324128hg38UCSC Ensembl
chr11:105747154..106194855hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38447701
hg19447702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468321
Supporting Variants
Samples
Known GenesAASDHPPT, GRIA4, KBTBD3, MSANTD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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