A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937063



Internal ID21357132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39044563..39044563hg38UCSC Ensembl
chr1:39510235..39510235hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192481
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937063
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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