A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191073



Internal ID22341835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26286561..26287142hg38UCSC Ensembl
chr2:26509429..26510010hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14288960, nssv14288959
SamplesHG00513, HG00514
Known GenesHADHB
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191073
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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