A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037263



Internal ID21946606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29130974..29134047hg38UCSC Ensembl
chr13:29705111..29708184hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg383074
hg193074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603327
Samples
Known GenesMTUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037263
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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