A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095072



Internal ID22004305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99332470..99332470hg38UCSC Ensembl
chr14:99798807..99798807hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095072
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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