A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14267703



Internal ID22121628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:48958091..48964275hg38UCSC Ensembl
Outerchr1:49423763..49429947hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg385613
hg195613
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216319
Supporting Variants
SamplesHG00512
Known GenesAGBL4
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14267703
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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