A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843



Internal ID15550693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:92897228..92942211hg38UCSC Ensembl
Outerchr7:92526542..92571525hg19UCSC Ensembl
Outerchr7:92364478..92409461hg18UCSC Ensembl
Outerchr7:92171193..92216176hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3844984
hg1944984
hg1844984
hg1744984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8402
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)nsv5843
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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