A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269367



Internal ID20478585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71553101..71553154hg38UCSC Ensembl
chr13:72127233..72127286hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736818
Supporting Variants
Samples
Known GenesDACH1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269367
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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