A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2108



Internal ID15541391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:54898273..54934879hg38UCSC Ensembl
Outerchr15:55190471..55227077hg19UCSC Ensembl
Outerchr15:52977763..53014369hg18UCSC Ensembl
Outerchr15:52977763..53014369hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3836607
hg1936607
hg1836607
hg1736607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1541
Supporting Variants
SamplesNA18555
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)nssv2108
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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