A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525092



Internal ID22394468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41278198..41278837hg38UCSC Ensembl
chr1:41743870..41744509hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv191n152
Supporting Variantsnssv14362471, nssv14362470
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525092
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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