A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321133



Internal ID20854236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66179241..66179963hg38UCSC Ensembl
chr1:66644924..66645646hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062536
Samples
Known GenesPDE4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321133
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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