A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902062



Internal ID22677216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140902540..140903508hg38UCSC Ensembl
chr3:140621382..140622350hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902062
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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