A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487405



Internal ID21144958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:43955791..44500132hg38UCSC Ensembl
chr14:44424994..44969335hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38544342
hg19544342
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2125n223
Supporting Variantsnssv18186817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487405
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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