A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1498



Internal ID15546061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:38362846..38396511hg38UCSC Ensembl
Outerchr15:38655047..38688712hg19UCSC Ensembl
Outerchr15:36442339..36476004hg18UCSC Ensembl
Outerchr15:36442339..36476004hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg386353
hg196353
hg186353
hg176353
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2930
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)nsv1498
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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