A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478348



Internal ID21135901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37606901..37629200hg38UCSC Ensembl
chr14:38076106..38098405hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3822300
hg1922300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2102n223
Supporting Variantsnssv18192132
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478348
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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