A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5821



Internal ID15550669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:84530397..84575152hg38UCSC Ensembl
Outerchr7:84159713..84204468hg19UCSC Ensembl
Outerchr7:83997649..84042404hg18UCSC Ensembl
Outerchr7:83804364..83849119hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3844756
hg1944756
hg1844756
hg1744756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8394
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv5821
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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