A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3231079



Internal ID22372122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:715641..745827hg38UCSC Ensembl
Outerchr10:761581..791767hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg384410
hg194410
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253499, nssv14253498
SamplesHG00732, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3231079
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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