A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10879



Internal ID15195233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:104974346..104991008hg38UCSC Ensembl
Outerchr12:105368124..105384786hg19UCSC Ensembl
Outerchr12:103892254..103908916hg18UCSC Ensembl
Outerchr12:103870591..103887253hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3816663
hg1916663
hg1816663
hg1716663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv869
Supporting Variants
SamplesNA18956
Known GenesC12orf45
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)nssv10879
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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