A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9991



Internal ID15195222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:51333395..51352515hg38UCSC Ensembl
Outerchr13:51907531..51926651hg19UCSC Ensembl
Outerchr13:50805532..50824652hg18UCSC Ensembl
Outerchr13:50805532..50824652hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg388719
hg198719
hg188719
hg178719
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041
Supporting Variants
SamplesNA18956
Known GenesMIR5693, SERPINE3
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)nssv9991
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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