A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212722



Internal ID22359888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133217338..133236988hg38UCSC Ensembl
chr10:135030842..135050492hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3819651
hg1919651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1168n152
Supporting Variantsnssv14389293
SamplesNA19240
Known GenesKNDC1, UTF1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212722
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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