A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990346



Internal ID20557386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30625823..30626208hg38UCSC Ensembl
chr11:30647370..30647755hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990346
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00081


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