A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095815



Internal ID22005048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24212585..24212585hg38UCSC Ensembl
chr14:24681791..24681791hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600538
Samples
Known GenesCHMP4A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095815
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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