A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221734



Internal ID22366014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:94060584..94110909hg38UCSC Ensembl
Outerchr7:93689896..93740221hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3850326
hg1950326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277797
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221734
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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