A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3237732



Internal ID22373957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:31067456..31070724hg38UCSC Ensembl
Outerchr17:29394474..29397742hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3824792
hg1924792
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14262256
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3237732
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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