A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1652



Internal ID15199529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:87829569..87863160hg38UCSC Ensembl
Outerchr15:88372800..88406391hg19UCSC Ensembl
Outerchr15:86173804..86207395hg18UCSC Ensembl
Outerchr15:86173804..86207395hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg386424
hg196424
hg186424
hg176424
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2942
SamplesNA18555
Known Genes
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)nsv1652
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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