A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225021



Internal ID22365003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:26281629..26290465hg38UCSC Ensembl
Outerchr7:26321249..26330085hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14280269
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225021
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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