A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480937



Internal ID21138490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87240101..87246100hg38UCSC Ensembl
chr14:87706445..87712444hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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