A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579825



Internal ID21771868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102180664..102183804hg38UCSC Ensembl
chr11:102051395..102054535hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383141
hg193141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029426
Supporting Variants
Samples
Known GenesYAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579825
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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