A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987363



Internal ID20554405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126945770..126946278hg38UCSC Ensembl
chr11:126815666..126816174hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459567
Supporting Variants
Samples
Known GenesKIRREL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00052


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