A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10039



Internal ID15542758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20360365..20390631hg38UCSC Ensembl
Outerchr15:20565618..20595884hg19UCSC Ensembl
Outerchr15:18825632..18855898hg18UCSC Ensembl
Outerchr15:18825632..18855898hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3830267
hg1930267
hg1830267
hg1730267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1452
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)nssv10039
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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