A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5192



Internal ID15544098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136724538..136738203hg38UCSC Ensembl
Outerchr9:139618990..139632655hg19UCSC Ensembl
Outerchr9:138738811..138752476hg18UCSC Ensembl
Outerchr9:136894827..136908492hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3824144
hg1924144
hg1824144
hg1724144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6769
Supporting Variants
SamplesNA19129
Known GenesFAM69B, LCN10, SNHG7, SNORA17, SNORA43
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)nssv5192
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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