A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583622



Internal ID21775665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69710926..69714566hg38UCSC Ensembl
chr11:69525694..69529334hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg383641
hg193641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023427
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583622
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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