A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8867



Internal ID15188311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:129333411..129378742hg38UCSC Ensembl
Outerchr10:131131675..131177006hg19UCSC Ensembl
Outerchr10:131021665..131066996hg18UCSC Ensembl
Outerchr10:131021665..131066996hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3845332
hg1945332
hg1845332
hg1745332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7616
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)nssv8867
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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