A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14279098



Internal ID22185595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:7028672..7039073hg38UCSC Ensembl
Outerchr10:7070634..7081035hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3810402
hg1910402
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220613
Supporting Variants
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14279098
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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