A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199314



Internal ID22348916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:167118968..167131559hg38UCSC Ensembl
Outerchr6:167532456..167545047hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3812592
hg1912592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14276030
SamplesNA19238
Known GenesCCR6
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199314
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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