A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076654



Internal ID21985887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156895744..156895744hg38UCSC Ensembl
chr4:157816896..157816896hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550944
Samples
Known GenesPDGFC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076654
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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