A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332391



Internal ID20865562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22848470..22855555hg38UCSC Ensembl
chr1:23174963..23182048hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg387086
hg197086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059211
Samples
Known GenesEPHB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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