A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220945



Internal ID22365489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125707857..125717928hg38UCSC Ensembl
Outerchr10:127396426..127406497hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3810072
hg1910072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14280992
SamplesHG00732
Known GenesFLJ37035, LOC283038
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220945
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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