A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224986



Internal ID22368255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101241792..101244074hg38UCSC Ensembl
chr13:101894143..101896425hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382283
hg192283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14369750
SamplesHG00733
Known GenesNALCN
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224986
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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