A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215490



Internal ID22361804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:31133170..31172494hg38UCSC Ensembl
Outerchr10:31422099..31461423hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3839325
hg1939325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14278634, nssv14278635
SamplesHG00512, HG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215490
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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