A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3244009



Internal ID22375740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:81205627..81212536hg38UCSC Ensembl
Outerchr10:82965383..82972292hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg382587
hg192587
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252666, nssv14252662, nssv14252664, nssv14252660, nssv14252661, nssv14252663, nssv14252658, nssv14252665, nssv14252659
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3244009
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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