A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872584



Internal ID22647524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22809634..22809866hg38UCSC Ensembl
chr1:23136127..23136359hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366148
Samples
Known GenesEPHB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872584
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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