A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476720



Internal ID21134273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:43666701..43801800hg38UCSC Ensembl
chr14:44135904..44271003hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38135100
hg19135100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2123n223
Supporting Variantsnssv18189982
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476720
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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