A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv871



Internal ID15552892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:106013738..106036028hg38UCSC Ensembl
Outerchr12:106407516..106429806hg19UCSC Ensembl
Outerchr12:104931646..104953936hg18UCSC Ensembl
Outerchr12:104909983..104932273hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3822291
hg1922291
hg1822291
hg1722291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9075
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)nsv871
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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