A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10921



Internal ID15539509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105764507..105932388hg38UCSC Ensembl
Outerchr14:106230844..106398248hg19UCSC Ensembl
Outerchr14:105301889..105469293hg18UCSC Ensembl
Outerchr14:105301889..105469293hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38167882
hg19167405
hg18167405
hg17167405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA15510
Known GenesKIAA0125
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)nssv10921
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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