A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867809



Internal ID22642744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220817516..220817579hg38UCSC Ensembl
chr1:220990858..220990921hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867809
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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