A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14276472



Internal ID22260800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:75912297..75923681hg38UCSC Ensembl
Outerchr10:77672055..77683439hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3811385
hg1911385
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218736
Supporting Variants
SamplesNA19238
Known GenesC10orf11
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14276472
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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