A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3231213



Internal ID22372173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134656629..134691202hg38UCSC Ensembl
Outerchr9:137548475..137583048hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382003
hg192003
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9798n152
Supporting Variantsnssv14253098, nssv14253097, nssv14253096
SamplesHG00512, HG00732, HG00733
Known GenesCOL5A1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3231213
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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