A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209982



Internal ID22357973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74631232..74631467hg38UCSC Ensembl
chr7:74045548..74045783hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14337312, nssv14337311, nssv14337309, nssv14337310
SamplesHG00512, HG00732, HG00733, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209982
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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