A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10059



Internal ID15542738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:66871200..66917407hg38UCSC Ensembl
Outerchr15:67163538..67209745hg19UCSC Ensembl
Outerchr15:64950592..64996799hg18UCSC Ensembl
Outerchr15:64950592..64996799hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3846208
hg1946208
hg1846208
hg1746208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1575
Supporting Variants
SamplesNA18956
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)nssv10059
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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