A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589013



Internal ID21781056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7407348..7407679hg38UCSC Ensembl
chr11:7428579..7428910hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040407
Supporting Variants
Samples
Known GenesSYT9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589013
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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