A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359480



Internal ID21017033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:630946..636491hg38UCSC Ensembl
chr4:624735..630280hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg385546
hg195546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119263
Samples
Known GenesPDE6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359480
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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