A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985



Internal ID15538712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:101693777..101712873hg38UCSC Ensembl
Outerchr11:101564508..101583604hg19UCSC Ensembl
Outerchr11:101069718..101088814hg18UCSC Ensembl
Outerchr11:101069718..101088814hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3819097
hg1919097
hg1819097
hg1719097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv461
Supporting Variants
SamplesNA12878
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)nssv3985
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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