A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484258



Internal ID21141811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24040605..24044683hg38UCSC Ensembl
chr14:24509814..24513892hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg384079
hg194079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016795
Samples
Known GenesDHRS4L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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