A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9221



Internal ID15187957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:78166701..78211375hg38UCSC Ensembl
Outerchr14:78633044..78677718hg19UCSC Ensembl
Outerchr14:77702797..77747471hg18UCSC Ensembl
Outerchr14:77702797..77747471hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3844675
hg1944675
hg1844675
hg1744675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1366
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)nssv9221
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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