A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075749



Internal ID21984982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165106953..165106953hg38UCSC Ensembl
chr4:166028105..166028105hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547731
Samples
Known GenesTMEM192
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075749
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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