A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3246168



Internal ID22376342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1456396..1467222hg38UCSC Ensembl
Outerchr10:1498591..1509417hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253477
SamplesHG00731
Known GenesADARB2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3246168
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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