A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480623



Internal ID21138176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81825701..81832100hg38UCSC Ensembl
chr14:82292045..82298444hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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