A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8663



Internal ID15188515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:122617748..122648067hg38UCSC Ensembl
Outerchr9:125380027..125410346hg19UCSC Ensembl
Outerchr9:124419848..124450167hg18UCSC Ensembl
Outerchr9:122459581..122489900hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg385404
hg195404
hg185404
hg175404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6705
Supporting Variants
SamplesNA12156
Known GenesOR1B1
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)nssv8663
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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