A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv730n152



Internal ID22816433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1535233..1546063hg38UCSC Ensembl
chr10:1577428..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 Variants
Supporting Variantsnsv3225234, nsv3228287
SamplesNA19239, HG00731, NA19240
Known GenesADARB2, ADARB2-AS1
MethodMerging
Optical mapping
AnalysisBioNano Genomics proprietary analysis
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformBioNano Genomics
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv730n152
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