A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6681



Internal ID15551615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:115131647..115176330hg38UCSC Ensembl
Outerchr9:117893926..117938609hg19UCSC Ensembl
Outerchr9:116933747..116978430hg18UCSC Ensembl
Outerchr9:114973480..115018163hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3844684
hg1944684
hg1844684
hg1744684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8655
SamplesNA12156
Known GenesDEC1
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)nsv6681
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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