A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262525



Internal ID20471743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93866424..93866493hg38UCSC Ensembl
chr11:93599590..93599659hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262525
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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