A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202197



Internal ID22351394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:102083401..102137832hg38UCSC Ensembl
Outerchr6:102531276..102585707hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3854432
hg1954432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14274790, nssv14274791
SamplesHG00731, HG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202197
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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