A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14267409



Internal ID22203864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:240623625..240647029hg38UCSC Ensembl
Outerchr2:241563042..241586446hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381886
hg191886
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218267
Supporting Variants
SamplesHG00732
Known GenesGPR35
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14267409
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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