A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994052



Internal ID20561092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83306656..83311714hg38UCSC Ensembl
chr11:83017699..83022757hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385059
hg195059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00038


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