A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1791



Internal ID15541074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88190840..88215827hg38UCSC Ensembl
Outerchr9:90805755..90830742hg19UCSC Ensembl
Outerchr9:89995575..90020562hg18UCSC Ensembl
Outerchr9:88035309..88060296hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3810006
hg1910006
hg1810006
hg1710006
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6603
Supporting Variants
SamplesNA18555
Known Genes
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)nssv1791
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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