A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561838



Internal ID22430606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57606185..57606185hg38UCSC Ensembl
chr1:58071857..58071857hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368819, nssv14368820
SamplesHG00732, HG00733
Known GenesDAB1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561838
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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