A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10360



Internal ID15542438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:129320541..129367654hg38UCSC Ensembl
Outerchr3:129039384..129086497hg19UCSC Ensembl
Outerchr3:130522074..130569187hg18UCSC Ensembl
Outerchr3:130522082..130569195hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3847114
hg1947114
hg1847114
hg1747114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3997
Supporting Variants
SamplesNA18956
Known GenesH1FX-AS1
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)nssv10360
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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