A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942774



Internal ID21362843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40800767..40800893hg38UCSC Ensembl
chr5:40800869..40800995hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196063
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942774
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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