A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498037



Internal ID20871245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93123419..93146983hg38UCSC Ensembl
chr14:93589764..93613328hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3823565
hg1923565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498037
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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