A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036364



Internal ID21945707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35694822..35697445hg38UCSC Ensembl
chr13:36268959..36271582hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg382624
hg192624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611683
Samples
Known GenesMIR548F5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036364
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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