A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9124



Internal ID15188054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:51325852..51349556hg38UCSC Ensembl
Outerchr13:51899988..51923692hg19UCSC Ensembl
Outerchr13:50797989..50821693hg18UCSC Ensembl
Outerchr13:50797989..50821693hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg385404
hg195404
hg185404
hg175404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041
Supporting Variants
SamplesNA12156
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)nssv9124
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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