A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990617



Internal ID20557658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32324601..32328800hg38UCSC Ensembl
chr11:32346147..32350346hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990617
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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