A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926815



Internal ID21346885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148178706..148178706hg38UCSC Ensembl
chr6:148499842..148499842hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202612
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926815
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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