A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490753



Internal ID21148306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58254343..58254850hg38UCSC Ensembl
chr14:58721061..58721568hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019882
Samples
Known GenesPSMA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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