A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7098



Internal ID15536766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:74713821..74746549hg38UCSC Ensembl
Outerchr4:75639032..75671759hg19UCSC Ensembl
Outerchr4:75858056..75890783hg18UCSC Ensembl
Outerchr4:75996211..76028938hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3832729
hg1932728
hg1832728
hg1732728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390
Supporting Variants
SamplesNA12156
Known GenesBTC
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)nssv7098
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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