A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488259



Internal ID21145812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35526039..35529805hg38UCSC Ensembl
chr14:35995245..35999011hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg383767
hg193767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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