A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202051



Internal ID22351263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235488099..235488578hg38UCSC Ensembl
chr2:236396743..236397222hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14297198, nssv14297199
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202051
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer