A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221337



Internal ID22365758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:34325902..34355817hg38UCSC Ensembl
Outerchr10:34614830..34644745hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3829916
hg1929916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14280002
SamplesHG00732
Known GenesPARD3
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221337
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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