A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501646



Internal ID20874883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102092088..102097088hg38UCSC Ensembl
chr14:102558425..102563425hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg385001
hg195001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182892
Samples
Known GenesHSP90AA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501646
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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