A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488254



Internal ID21145807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73713601..73714800hg38UCSC Ensembl
chr14:74180304..74181503hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020185
Samples
Known GenesPNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488254
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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