A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882052



Internal ID22657029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38967338..38975197hg38UCSC Ensembl
chr1:39433010..39440869hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg387860
hg197860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882052
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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