A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021296



Internal ID21930639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44456391..44456456hg38UCSC Ensembl
chr13:45030527..45030592hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616313
Samples
Known GenesTSC22D1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021296
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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