A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6464



Internal ID15537400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63426650..63446201hg38UCSC Ensembl
Outerchr11:63194122..63213673hg19UCSC Ensembl
Outerchr11:62950698..62970249hg18UCSC Ensembl
Outerchr11:62950698..62970249hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3819552
hg1919552
hg1819552
hg1719552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv350
Supporting Variants
SamplesNA12156
Known GenesMIR3680-1, MIR3680-2
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)nssv6464
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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