A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14275655



Internal ID22262669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:6547784..6573063hg38UCSC Ensembl
Outerchr5:6547897..6573176hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg384299
hg194299
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213001
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14275655
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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