A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879669



Internal ID22654641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167603917..167604546hg38UCSC Ensembl
chr1:167573154..167573783hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879669
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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