A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2869



Internal ID15195005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63556283..63563389hg38UCSC Ensembl
Outerchr11:63323755..63330861hg19UCSC Ensembl
Outerchr11:63080331..63087437hg18UCSC Ensembl
Outerchr11:63080331..63087437hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg386474
hg196474
hg186474
hg176474
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv352
Supporting Variants
SamplesNA18555
Known GenesHRASLS2
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)nssv2869
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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