A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501641



Internal ID20874878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94856110..94870767hg38UCSC Ensembl
chr14:95322447..95337104hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3814658
hg1914658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501641
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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