A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1252



Internal ID15544474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:54826027..54858545hg38UCSC Ensembl
Outerchr15:55118225..55150743hg19UCSC Ensembl
Outerchr15:52905517..52938035hg18UCSC Ensembl
Outerchr15:52905517..52938035hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg388474
hg198474
hg188474
hg178474
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1540
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)nssv1252
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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