A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226456



Internal ID22369249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99535434..99535528hg38UCSC Ensembl
chr10:101295191..101295285hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1027n152
Supporting Variantsnssv14384254
SamplesNA19240
Known GenesNKX2-3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226456
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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