A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1471



Internal ID15546034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:27778792..27798658hg38UCSC Ensembl
Outerchr15:28023938..28043804hg19UCSC Ensembl
Outerchr15:25697533..25717399hg18UCSC Ensembl
Outerchr15:25697533..25717399hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3819867
hg1919867
hg1819867
hg1719867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2103
SamplesNA18555
Known GenesOCA2
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)nsv1471
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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