A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608369



Internal ID21800416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127752717..127786092hg38UCSC Ensembl
chr11:127622612..127655987hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3833376
hg1933376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608369
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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