A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202627



Internal ID22351764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26655037..26693179hg38UCSC Ensembl
Outerchr6:26655265..26693407hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3838143
hg1938143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14276111, nssv14276110
SamplesNA19239, NA19240
Known GenesZNF322
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202627
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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