A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202988



Internal ID22352074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:15799895..15811686hg38UCSC Ensembl
Outerchr3:15841402..15853193hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3811792
hg1911792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14270357, nssv14270355, nssv14270356
SamplesNA19238, HG00513, HG00514
Known GenesANKRD28
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202988
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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