A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8878



Internal ID15534986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:8750430..8784550hg38UCSC Ensembl
Outerchr11:8771977..8806097hg19UCSC Ensembl
Outerchr11:8728553..8762673hg18UCSC Ensembl
Outerchr11:8728553..8762673hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385312
hg195312
hg185312
hg175312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7664
Supporting Variants
SamplesNA12156
Known GenesST5
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)nssv8878
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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