A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205466



Internal ID22354153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:137849726..137920338hg38UCSC Ensembl
Outerchr3:137568568..137639180hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3870613
hg1970613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14270825
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205466
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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