A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091842



Internal ID22001075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71076018..71076018hg38UCSC Ensembl
chr14:71542735..71542735hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598856
Samples
Known GenesPCNX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091842
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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