A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266868



Internal ID20476086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71502311..71502506hg38UCSC Ensembl
chr11:71213357..71213552hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747262
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266868
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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