A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10026



Internal ID15542771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:72298712..72357703hg38UCSC Ensembl
Outerchr1:72764395..72823386hg19UCSC Ensembl
Outerchr1:72536983..72595974hg18UCSC Ensembl
Outerchr1:72476416..72535407hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3858992
hg1958992
hg1858992
hg1758992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1376
Supporting Variants
SamplesNA18956
Known Genes
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)nssv10026
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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