A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202359



Internal ID22351537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17706817..17713473hg38UCSC Ensembl
chr7:17746441..17753097hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg386657
hg196657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14334919
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202359
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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