A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219859



Internal ID22364741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:2890921..2912607hg38UCSC Ensembl
Outerchr19:2890919..2912605hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3821687
hg1921687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14263358
SamplesHG00731
Known GenesZNF57
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219859
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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