A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222424



Internal ID22366501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69409867..69409918hg38UCSC Ensembl
chr10:71169623..71169674hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv976n152
Supporting Variantsnssv14352541, nssv14352540, nssv14352538, nssv14352539
SamplesNA19238, HG00731, HG00732, HG00733
Known GenesTACR2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222424
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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