A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207897



Internal ID22356226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:71255973..71272555hg38UCSC Ensembl
Outerchr6:71965676..71982258hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3816583
hg1916583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14274838, nssv14274837
SamplesHG00732, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207897
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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