A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1597



Internal ID15546160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:71255429..71290146hg38UCSC Ensembl
Outerchr15:71547768..71582485hg19UCSC Ensembl
Outerchr15:69334822..69369539hg18UCSC Ensembl
Outerchr15:69334822..69369539hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385310
hg195310
hg185310
hg175310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2940
SamplesNA18555
Known GenesTHSD4
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)nsv1597
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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