A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5563



Internal ID15197204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:72257544..72292835hg38UCSC Ensembl
Outerchr15:72549885..72585176hg19UCSC Ensembl
Outerchr15:70336939..70372230hg18UCSC Ensembl
Outerchr15:70336939..70372230hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3835292
hg1935292
hg1835292
hg1735292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1601
Supporting Variants
SamplesNA19129
Known GenesCELF6, PARP6
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)nssv5563
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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