A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885453



Internal ID22660437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36568268..36573641hg38UCSC Ensembl
chr1:37033869..37039242hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385374
hg195374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885453
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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