A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6688



Internal ID15551622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:116430327..116475537hg38UCSC Ensembl
Outerchr9:119192606..119237816hg19UCSC Ensembl
Outerchr9:118232427..118277637hg18UCSC Ensembl
Outerchr9:116272160..116317370hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3845211
hg1945211
hg1845211
hg1745211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8658
SamplesNA12156
Known GenesASTN2
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)nsv6688
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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