A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5151



Internal ID15542935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:14819689..14851744hg38UCSC Ensembl
Outerchr9:14819687..14851742hg19UCSC Ensembl
Outerchr9:14809687..14841742hg18UCSC Ensembl
Outerchr9:14809687..14841742hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg387229
hg197229
hg187229
hg177229
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484
Supporting Variants
SamplesNA19129
Known GenesFREM1
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)nssv5151
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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