A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199359



Internal ID22348954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:149435614..149519592hg38UCSC Ensembl
Outerchr4:150356766..150440744hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3883979
hg1983979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14272824
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199359
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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