A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1596



Internal ID15199473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:71125691..71159112hg38UCSC Ensembl
Outerchr15:71418030..71451451hg19UCSC Ensembl
Outerchr15:69205084..69238505hg18UCSC Ensembl
Outerchr15:69205084..69238505hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3833422
hg1933422
hg1833422
hg1733422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7194
SamplesNA12156
Known GenesTHSD4
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)nsv1596
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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