A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10811



Internal ID15541987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:26146514..26178526hg38UCSC Ensembl
Outerchr11:26168061..26200073hg19UCSC Ensembl
Outerchr11:26124637..26156649hg18UCSC Ensembl
Outerchr11:26124637..26156649hg17UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg387497
hg197497
hg187497
hg177497
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7719
Supporting Variants
SamplesNA18956
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)nssv10811
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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