A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3240737



Internal ID22374775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:90645876..90658956hg38UCSC Ensembl
Outerchr15:91189107..91202187hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382813
hg192813
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258878, nssv14258879, nssv14258880
SamplesNA19238, NA19240, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3240737
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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