A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212649



Internal ID22359828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98407737..98407796hg38UCSC Ensembl
chr10:100167494..100167553hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1024n152
Supporting Variantsnssv14439901, nssv14413050
SamplesHG00733, HG00514
Known GenesPYROXD2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212649
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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