A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9171



Internal ID15188007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:20652709..20697918hg38UCSC Ensembl
Outerchr14:21120868..21166077hg19UCSC Ensembl
Outerchr14:20190708..20235917hg18UCSC Ensembl
Outerchr14:20190708..20235917hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3845210
hg1945210
hg1845210
hg1745210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1203
Supporting Variants
SamplesNA12156
Known GenesANG, RNASE4
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)nssv9171
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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