A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529880



Internal ID22399271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44414530..44414584hg38UCSC Ensembl
chr10:44909978..44910032hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14345051, nssv14345053, nssv14345052
SamplesHG00732, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529880
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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