A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10835



Internal ID15541963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:101694899..101706165hg38UCSC Ensembl
Outerchr11:101565630..101576896hg19UCSC Ensembl
Outerchr11:101070840..101082106hg18UCSC Ensembl
Outerchr11:101070840..101082106hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3811267
hg1911267
hg1811267
hg1711267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv461
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)nssv10835
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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