A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5187



Internal ID15544123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133189444..133220843hg38UCSC Ensembl
Outerchr9:136064831..136096230hg19UCSC Ensembl
Outerchr9:135054652..135086051hg18UCSC Ensembl
Outerchr9:133094385..133125784hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg387866
hg197866
hg187866
hg177866
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6748
Supporting Variants
SamplesNA19129
Known GenesOBP2B
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)nssv5187
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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