A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1539



Internal ID15546102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:53190673..53226562hg38UCSC Ensembl
Outerchr15:53482870..53518759hg19UCSC Ensembl
Outerchr15:51270162..51306051hg18UCSC Ensembl
Outerchr15:51270162..51306051hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385642
hg195642
hg185642
hg175642
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5557, nssv1251
SamplesNA19240, NA19129
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)nsv1539
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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