A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585758



Internal ID21777801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81488324..81569136hg38UCSC Ensembl
chr11:81199366..81280178hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3880813
hg1980813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027934
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585758
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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