A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951698



Internal ID21371767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76427230..76427230hg38UCSC Ensembl
chr4:77348383..77348383hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201173
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951698
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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