A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9050



Internal ID15534814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:77171413..77196286hg38UCSC Ensembl
Outerchr12:77565193..77590066hg19UCSC Ensembl
Outerchr12:76089324..76114197hg18UCSC Ensembl
Outerchr12:76067661..76092534hg17UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3824874
hg1924874
hg1824874
hg1724874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv780
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)nssv9050
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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