A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879945



Internal ID22654916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160984072..160990920hg38UCSC Ensembl
chr1:160953862..160960710hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg386849
hg196849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879945
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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