A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14264677



Internal ID22134610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:71944097..71994216hg38UCSC Ensembl
Outerchr2:72171227..72221346hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3850120
hg1950120
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204912
Supporting Variants
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14264677
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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