A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210364



Internal ID22358296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:155402944..155412507hg38UCSC Ensembl
Outerchr7:155195639..155205202hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg389564
hg199564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14278807
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210364
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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