A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3241257



Internal ID22374920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32833254..32838333hg38UCSC Ensembl
chr1:33298855..33303934hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg385080
hg195080
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360871, nssv14360872, nssv14360873, nssv14360876, nssv14360870, nssv14360874, nssv14360875
SamplesNA19238, NA19239, HG00731, NA19240, HG00733, HG00513, HG00514
Known GenesS100PBP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3241257
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer