A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074136



Internal ID21983369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26652248..26652248hg38UCSC Ensembl
chr4:26653870..26653870hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544474
Samples
Known GenesTBC1D19
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074136
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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