A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3231201



Internal ID22372167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32862240..32866763hg38UCSC Ensembl
chr6:32830017..32834540hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384524
hg194524
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327158, nssv14327776, nssv14327157, nssv14327159, nssv14327777
SamplesHG00512, NA19238, HG00731, HG00732, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3231201
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