A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8417



Internal ID15535447
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 StatusS
Merged Variantsnsv5902
Supporting Variants
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)nssv8417
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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