A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1598



Internal ID15546161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:71359192..71381435hg38UCSC Ensembl
Outerchr15:71651531..71673774hg19UCSC Ensembl
Outerchr15:69438585..69460828hg18UCSC Ensembl
Outerchr15:69438585..69460828hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384844
hg194844
hg184844
hg174844
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4162
SamplesNA12878
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)nsv1598
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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