A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296399



Internal ID20505617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106570443..106570539hg38UCSC Ensembl
chr13:107222791..107222887hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737884
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296399
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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