A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205885



Internal ID22354509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:105077338..105105304hg38UCSC Ensembl
Outerchr1:105619960..105647926hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3827967
hg1927967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14266706
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205885
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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