A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1807



Internal ID15194405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133044293..133068877hg38UCSC Ensembl
Outerchr9:135919680..135944264hg19UCSC Ensembl
Outerchr9:134909501..134934085hg18UCSC Ensembl
Outerchr9:132949234..132973818hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3815418
hg1915418
hg1815418
hg1715418
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6746
Supporting Variants
SamplesNA18555
Known GenesCEL, GTF3C5, MIR6877
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)nssv1807
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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