A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926610



Internal ID21346679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119796374..119796374hg38UCSC Ensembl
chr4:120717529..120717529hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200009
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926610
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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