A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8976



Internal ID15188202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125918491..125963371hg38UCSC Ensembl
Outerchr11:125788386..125833266hg19UCSC Ensembl
Outerchr11:125293596..125338476hg18UCSC Ensembl
Outerchr11:125293596..125338476hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3844881
hg1944881
hg1844881
hg1744881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv535
Supporting Variants
SamplesNA12156
Known GenesCDON, DDX25
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)nssv8976
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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