A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8949



Internal ID15534915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93938969..93974375hg38UCSC Ensembl
Outerchr11:93672135..93707541hg19UCSC Ensembl
Outerchr11:93311783..93347189hg18UCSC Ensembl
Outerchr11:93311783..93347189hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3835407
hg1935407
hg1835407
hg1735407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv442
Supporting Variants
SamplesNA12156
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)nssv8949
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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