A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937620



Internal ID21357689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23731302..23731302hg38UCSC Ensembl
chr6:23731530..23731530hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202346
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937620
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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