A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205209



Internal ID22353936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:41306680..41321834hg38UCSC Ensembl
Outerchr6:41274418..41289572hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3815155
hg1915155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14274778
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205209
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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