A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210635



Internal ID22358471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:90827308..90867122hg38UCSC Ensembl
Outerchr11:90560476..90600290hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3839815
hg1939815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253580, nssv14253581
SamplesNA19238, NA19240
Known GenesDISC1FP1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210635
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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