A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384305



Internal ID21041858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41297198..41309125hg38UCSC Ensembl
chr5:41297300..41309227hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3811928
hg1911928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130969
Samples
Known GenesPLCXD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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