A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192895



Internal ID22343418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:28454077..28508625hg38UCSC Ensembl
Outerchr3:28495568..28550116hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3854549
hg1954549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271115
SamplesHG00513
Known GenesZCWPW2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192895
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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