A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928210



Internal ID21348279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179650349..179650476hg38UCSC Ensembl
chr5:179077350..179077477hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196786
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928210
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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