A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6733



Internal ID15204986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130261373..130284643hg38UCSC Ensembl
Outerchr9:133023652..133046922hg19UCSC Ensembl
Outerchr9:132063473..132086743hg18UCSC Ensembl
Outerchr9:130103206..130126476hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3823271
hg1923271
hg1823271
hg1723271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3753
SamplesNA12878
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)nsv6733
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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