A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988232



Internal ID20555272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134084781..134105505hg38UCSC Ensembl
chr11:133954676..133975400hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3820725
hg1920725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469161
Supporting Variants
Samples
Known GenesJAM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988232
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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