A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212851



Internal ID22359975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:97352362..97360156hg38UCSC Ensembl
Outerchr7:96981674..96989468hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg387795
hg197795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277420
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212851
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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