A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8022



Internal ID15189156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:163144457..163161504hg38UCSC Ensembl
Outerchr4:164065609..164082656hg19UCSC Ensembl
Outerchr4:164285059..164302106hg18UCSC Ensembl
Outerchr4:164423214..164440261hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3817048
hg1917048
hg1817048
hg1717048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4585
Supporting Variants
SamplesNA12156
Known GenesNAF1
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)nssv8022
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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