A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5556



Internal ID15543898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:51567486..51580356hg38UCSC Ensembl
Outerchr15:51859683..51872553hg19UCSC Ensembl
Outerchr15:49646975..49659845hg18UCSC Ensembl
Outerchr15:49646975..49659845hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386851
hg196851
hg186851
hg176851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1535
Supporting Variants
SamplesNA19129
Known GenesDMXL2
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)nssv5556
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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