A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475350



Internal ID21132903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:104112101..107043900hg38UCSC Ensembl
chr11:103982829..106914626hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382931800
hg192931798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986056
Samples
Known GenesAASDHPPT, CARD16, CARD17, CARD18, CASP1, CASP12, CASP4, CASP5, GRIA4, GUCY1A2, KBTBD3, LOC643733, MSANTD4, PDGFD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475350
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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