A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192726



Internal ID22343271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:159791..159880hg38UCSC Ensembl
chr7:159791..159880hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14332834
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192726
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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