A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221022



Internal ID22365547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4031226..4031302hg38UCSC Ensembl
chr10:4073418..4073494hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv757n152
Supporting Variantsnssv14461056
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)nsv3221022
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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