A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3246676



Internal ID22376484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:8419596..8424059hg38UCSC Ensembl
Outerchr19:8484480..8488943hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381516
hg191516
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14262577, nssv14262575, nssv14262576, nssv14262573, nssv14262571, nssv14262572, nssv14262574, nssv14262579, nssv14262578
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesMARCH2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3246676
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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