A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335025



Internal ID20868215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65876001..65876800hg38UCSC Ensembl
chr1:66341684..66342483hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062496
Samples
Known GenesPDE4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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