A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225234



Internal ID22368431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1535233..1546063hg38UCSC Ensembl
Outerchr10:1577428..1588258hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3810831
hg1910831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv730n152
Supporting Variantsnssv14277443, nssv14277444, nssv14277442
SamplesNA19239, HG00731, NA19240
Known GenesADARB2, ADARB2-AS1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225234
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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