A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199650



Internal ID22349207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:14963403..14974125hg38UCSC Ensembl
Outerchr3:15004910..15015632hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3810723
hg1910723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271657
SamplesNA19239
Known GenesNR2C2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199650
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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