A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025739



Internal ID21935082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113600655..113600747hg38UCSC Ensembl
chr13:114254970..114255062hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598053
Samples
Known GenesTFDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025739
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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