A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209804



Internal ID22357824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240961618..240961783hg38UCSC Ensembl
chr2:241901035..241901200hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14298811, nssv14298810
SamplesHG00512, HG00514
Known GenesLOC200772
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209804
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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