A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9507



Internal ID15193121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:73527798..73569132hg38UCSC Ensembl
Outerchr14:73994502..74035836hg19UCSC Ensembl
Outerchr14:73064255..73105589hg18UCSC Ensembl
Outerchr14:73064255..73105589hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3841335
hg1941335
hg1841335
hg1741335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1350
Supporting Variants
SamplesNA18507
Known GenesACOT1, ACOT2, HEATR4
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)nssv9507
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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