A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218168



Internal ID22363600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98591503..98605952hg38UCSC Ensembl
Outerchr7:98220815..98235264hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3814450
hg1914450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277798
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218168
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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