A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202037



Internal ID22351251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129181240..129181652hg38UCSC Ensembl
chr3:128900083..128900495hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308636, nssv14308637, nssv14308635
SamplesHG00731, HG00732, HG00733
Known GenesCNBP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202037
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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