A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223799



Internal ID22367463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6000959..6001134hg38UCSC Ensembl
chr10:6042922..6043097hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv766n152
Supporting Variantsnssv14459953
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223799
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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