A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200878



Internal ID22350267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:9159252..9171092hg38UCSC Ensembl
Outerchr1:9219311..9231151hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3811841
hg1911841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14257845
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200878
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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