A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9173



Internal ID15534691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:20921418..20954858hg38UCSC Ensembl
Outerchr14:21389577..21423017hg19UCSC Ensembl
Outerchr14:20459417..20492857hg18UCSC Ensembl
Outerchr14:20459417..20492857hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg385994
hg195994
hg185994
hg175994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1206
Supporting Variants
SamplesNA12156
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)nssv9173
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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