A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9222



Internal ID15534642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:78601178..78640044hg38UCSC Ensembl
Outerchr14:79067521..79106387hg19UCSC Ensembl
Outerchr14:78137274..78176140hg18UCSC Ensembl
Outerchr14:78137274..78176140hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3838867
hg1938867
hg1838867
hg1738867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1367
Supporting Variants
SamplesNA12156
Known GenesNRXN3
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)nssv9222
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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