A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487108



Internal ID21144661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58578336..58589942hg38UCSC Ensembl
chr14:59045054..59056660hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3811607
hg1911607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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