A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934026



Internal ID21354095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158473767..158473767hg38UCSC Ensembl
chr1:158443557..158443557hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187080
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934026
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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