A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902



Internal ID15550758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:112312073..112357210hg38UCSC Ensembl
Outerchr7:111952128..111997265hg19UCSC Ensembl
Outerchr7:111739364..111784501hg18UCSC Ensembl
Outerchr7:111546079..111591216hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3845138
hg1945138
hg1845138
hg1745138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8417
SamplesNA12156
Known GenesZNF277
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)nsv5902
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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