A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9224



Internal ID15187954
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 StatusS
Merged Variantsnsv1154
Supporting Variants
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)nssv9224
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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