A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9939



Internal ID15193341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1523000..1549085hg38UCSC Ensembl
Outerchr11:1544230..1570315hg19UCSC Ensembl
Outerchr11:1500806..1526891hg18UCSC Ensembl
Outerchr11:1500806..1526891hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387602
hg197602
hg187602
hg177602
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7640
Supporting Variants
SamplesNA18507
Known GenesMOB2
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)nssv9939
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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