A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943951



Internal ID21364020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:789481..789481hg38UCSC Ensembl
chr1:724861..724861hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg382364
hg192364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194121
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943951
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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