A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9231



Internal ID15534633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:92986885..93018806hg38UCSC Ensembl
Outerchr14:93453230..93485151hg19UCSC Ensembl
Outerchr14:92522983..92554904hg18UCSC Ensembl
Outerchr14:92522983..92554904hg17UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3831922
hg1931922
hg1831922
hg1731922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1401
Supporting Variants
SamplesNA12156
Known GenesITPK1
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)nssv9231
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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