A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5551



Internal ID15543903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:42174345..42206261hg38UCSC Ensembl
Outerchr15:42466543..42498459hg19UCSC Ensembl
Outerchr15:40253835..40285751hg18UCSC Ensembl
Outerchr15:40253835..40285751hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg387370
hg197370
hg187370
hg177370
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1507
Supporting Variants
SamplesNA19129
Known GenesMIR627, VPS39
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)nssv5551
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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