A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036071



Internal ID21945414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113593557..113593901hg38UCSC Ensembl
chr13:114247872..114248216hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597845
Samples
Known GenesTFDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036071
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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