A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949555



Internal ID21369624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119010728..119010728hg38UCSC Ensembl
chr1:119553351..119553351hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185629
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949555
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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