A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867730



Internal ID22642666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29387017..29390644hg38UCSC Ensembl
chr1:29713529..29717156hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383628
hg193628
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867730
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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