A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8858



Internal ID15535006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125236944..125263916hg38UCSC Ensembl
Outerchr10:126925513..126952485hg19UCSC Ensembl
Outerchr10:126915503..126942475hg18UCSC Ensembl
Outerchr10:126915503..126942475hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3826973
hg1926973
hg1826973
hg1726973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7595
Supporting Variants
SamplesNA12156
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)nssv8858
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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