A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215177



Internal ID22361595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23790542..23790673hg38UCSC Ensembl
chr10:24079471..24079602hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv837n152
Supporting Variantsnssv14410722
SamplesNA19240
Known GenesKIAA1217
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215177
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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