A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505091



Internal ID20878357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104949301..104953100hg38UCSC Ensembl
chr14:105415638..105419437hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2262n223
Supporting Variantsnssv18194356
Samples
Known GenesAHNAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505091
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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