A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266428



Internal ID20475646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32233616..32233731hg38UCSC Ensembl
chr10:32522544..32522659hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746493
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266428
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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