A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936314



Internal ID21356383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108689608..108689608hg38UCSC Ensembl
chr1:109232230..109232230hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185468
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936314
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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