A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9513



Internal ID15539801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:39497017..39519262hg38UCSC Ensembl
Outerchr15:39789218..39811463hg19UCSC Ensembl
Outerchr15:37576510..37598755hg18UCSC Ensembl
Outerchr15:37576510..37598755hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3814452
hg1914452
hg1814452
hg1714452
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1501
Supporting Variants
SamplesNA18507
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)nssv9513
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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