A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192799



Internal ID22343333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:57971400..58004969hg38UCSC Ensembl
Outerchr3:57957127..57990696hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3833570
hg1933570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14270901
SamplesHG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192799
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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