A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1553



Internal ID15546116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:59917162..59942744hg38UCSC Ensembl
Outerchr15:60209361..60234943hg19UCSC Ensembl
Outerchr15:57996653..58022235hg18UCSC Ensembl
Outerchr15:57996653..58022235hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3825583
hg1925583
hg1825583
hg1725583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7176
SamplesNA12156
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)nsv1553
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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