A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562559



Internal ID22392880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231604674..231604674hg38UCSC Ensembl
chr2:232469385..232469385hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14298986
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562559
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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