A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591069



Internal ID21783112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66633646..66633708hg38UCSC Ensembl
chr11:66401117..66401179hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034818
Supporting Variants
Samples
Known GenesRBM14-RBM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591069
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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