A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11235



Internal ID15539344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6351101..6380854hg38UCSC Ensembl
Outerchr10:6393063..6422816hg19UCSC Ensembl
Outerchr10:6433069..6462822hg18UCSC Ensembl
Outerchr10:6433069..6462822hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3829754
hg1929754
hg1829754
hg1729754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5676
Supporting Variants
SamplesNA15510
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)nssv11235
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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