A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220557



Internal ID22365218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:44197700..44204893hg38UCSC Ensembl
Outerchr21:45617583..45624776hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg387194
hg197194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14267862, nssv14267863
SamplesHG00512, NA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220557
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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