A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1236



Internal ID15544491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20372666..20394125hg38UCSC Ensembl
Outerchr15:20577919..20599378hg19UCSC Ensembl
Outerchr15:18837933..18859392hg18UCSC Ensembl
Outerchr15:18837933..18859392hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3821460
hg1921460
hg1821460
hg1721460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1452
Supporting Variants
SamplesNA19240
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)nssv1236
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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