A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225824



Internal ID22368837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74585..74947hg38UCSC Ensembl
chr10:120525..120887hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14322229
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225824
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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