A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221903



Internal ID22366139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:140992002..141003582hg38UCSC Ensembl
Outerchr7:140691802..140703382hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3811581
hg1911581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277803
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221903
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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