A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv868



Internal ID15206203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:104465186..104501794hg38UCSC Ensembl
Outerchr12:104858964..104895572hg19UCSC Ensembl
Outerchr12:103383094..103419702hg18UCSC Ensembl
Outerchr12:103361431..103398039hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3836609
hg1936609
hg1836609
hg1736609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9074
SamplesNA12156
Known GenesCHST11
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)nsv868
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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