A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5322



Internal ID15196635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:118578807..118611109hg38UCSC Ensembl
Outerchr10:120338319..120370621hg19UCSC Ensembl
Outerchr10:120328309..120360611hg18UCSC Ensembl
Outerchr10:120328309..120360611hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg386984
hg196984
hg186984
hg176984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7569
Supporting Variants
SamplesNA19129
Known GenesPRLHR
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)nssv5322
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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