A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8168



Internal ID15189010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:151678840..151711904hg38UCSC Ensembl
Outerchr5:151058401..151091465hg19UCSC Ensembl
Outerchr5:151038594..151071658hg18UCSC Ensembl
Outerchr5:151038594..151071658hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg386376
hg196376
hg186376
hg176376
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5069
Supporting Variants
SamplesNA12156
Known GenesSPARC
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)nssv8168
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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