A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872137



Internal ID22647076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232259666..232265703hg38UCSC Ensembl
chr1:232395412..232401449hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg386038
hg196038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363214
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872137
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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