A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755716



Internal ID20531576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104603521..104603521hg38UCSC Ensembl
chr14:105069858..105069858hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276334
Samples
Known GenesTMEM179
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755716
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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