A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14280834



Internal ID22133287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35103023..35191678hg38UCSC Ensembl
Outerchr10:35391951..35480606hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3888656
hg1988656
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228043
Supporting Variants
SamplesHG00513
Known GenesCREM
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14280834
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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