A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9066



Internal ID15188112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:98825781..98837212hg38UCSC Ensembl
Outerchr12:99219559..99230990hg19UCSC Ensembl
Outerchr12:97743690..97755121hg18UCSC Ensembl
Outerchr12:97722027..97733458hg17UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3811432
hg1911432
hg1811432
hg1711432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv845
Supporting Variants
SamplesNA12156
Known GenesANKS1B
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)nssv9066
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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