A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479090



Internal ID21136643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82753810..82766035hg38UCSC Ensembl
chr14:83220154..83232379hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3812226
hg1912226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021494
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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