A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215786



Internal ID22361998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:91784941..91814409hg38UCSC Ensembl
Outerchr9:94547223..94576691hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3829469
hg1929469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281972, nssv14281973, nssv14281971, nssv14281970
SamplesHG00512, HG00732, NA19240, HG00514
Known GenesROR2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215786
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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