A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4142



Internal ID15538869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:27581763..27616658hg38UCSC Ensembl
Outerchr15:27826909..27861804hg19UCSC Ensembl
Outerchr15:25500504..25535399hg18UCSC Ensembl
Outerchr15:25500504..25535399hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg384850
hg194850
hg184850
hg174850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1469
Supporting Variants
SamplesNA12878
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)nssv4142
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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