A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985437



Internal ID20552477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101894682..101910197hg38UCSC Ensembl
chr11:101765413..101780928hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3815516
hg1915516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474867
Supporting Variants
Samples
Known GenesANGPTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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