A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220476



Internal ID22365159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73777842..73778150hg38UCSC Ensembl
chr10:75537600..75537908hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354351, nssv14354354, nssv14354350, nssv14354352, nssv14354353
SamplesHG00512, NA19239, HG00731, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220476
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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