A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204914



Internal ID22353692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26153223..26155996hg38UCSC Ensembl
chr2:26376092..26378865hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg382774
hg192774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14288943
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204914
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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