A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3237737



Internal ID22373958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:7423828..7445282hg38UCSC Ensembl
Outerchr9:7423828..7445282hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381491
hg191491
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282298, nssv14282296, nssv14282297
SamplesNA19238, HG00732, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3237737
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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