A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv856



Internal ID15552877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:100962494..100995537hg38UCSC Ensembl
Outerchr12:101356272..101389315hg19UCSC Ensembl
Outerchr12:99880403..99913446hg18UCSC Ensembl
Outerchr12:99858740..99891783hg17UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg386396
hg196396
hg186396
hg176396
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9070
SamplesNA12156
Known GenesANO4
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)nsv856
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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