A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202603



Internal ID22351744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:16881295..16897938hg38UCSC Ensembl
Outerchr6:16881526..16898169hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3816644
hg1916644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14274815
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202603
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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