A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14264002



Internal ID22196752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:6287224..6326926hg38UCSC Ensembl
Outerchr19:6287235..6326937hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3244196
Supporting Variants
SamplesHG00731
Known GenesACER1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14264002
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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