A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1835



Internal ID15541118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:940902..985412hg38UCSC Ensembl
Outerchr10:986842..1031352hg19UCSC Ensembl
Outerchr10:976842..1021352hg18UCSC Ensembl
Outerchr10:976842..1021352hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3844511
hg1944511
hg1844511
hg1744511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521
Supporting Variants
SamplesNA18555
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)nssv1835
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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