A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1015



Internal ID15544770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:66159667..66181322hg38UCSC Ensembl
Outerchr11:65927138..65948793hg19UCSC Ensembl
Outerchr11:65683714..65705369hg18UCSC Ensembl
Outerchr11:65683714..65705369hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3821656
hg1921656
hg1821656
hg1721656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv362
Supporting Variants
SamplesNA19240
Known GenesPACS1
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)nssv1015
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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