A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926903



Internal ID21346974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:123236804..123237327hg38UCSC Ensembl
chr5:122572498..122573021hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196743
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926903
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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