A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597367



Internal ID21789410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11854051..11855010hg38UCSC Ensembl
chr11:11875598..11876557hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033603
Supporting Variants
Samples
Known GenesUSP47
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597367
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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