A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525644



Internal ID22395022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128953526..128956228hg38UCSC Ensembl
chr3:128672369..128675071hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308630, nssv14308628, nssv14308629
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525644
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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