A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154



Internal ID15199031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:63928656..63963054hg38UCSC Ensembl
Outerchr1:64394327..64428725hg19UCSC Ensembl
Outerchr1:64166915..64201313hg18UCSC Ensembl
Outerchr1:64106348..64140746hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3834399
hg1934399
hg1834399
hg1734399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9224
SamplesNA12156
Known GenesROR1
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)nsv1154
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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