A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482081



Internal ID21139634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24220599..24223841hg38UCSC Ensembl
chr14:24689805..24693047hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016803
Samples
Known GenesNEDD8, NEDD8-MDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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