A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316357



Internal ID20849436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66158770..66165623hg38UCSC Ensembl
chr1:66624453..66631306hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg386854
hg196854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062534
Samples
Known GenesPDE4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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