A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14260581



Internal ID22256637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:19707954..19713863hg38UCSC Ensembl
Outerchr17:19611267..19617176hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3239486
Supporting Variants
SamplesNA19238
Known GenesSLC47A2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14260581
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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