A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3915



Internal ID15191956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1534592..1549430hg38UCSC Ensembl
Outerchr11:1555822..1570660hg19UCSC Ensembl
Outerchr11:1512398..1527236hg18UCSC Ensembl
Outerchr11:1512398..1527236hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg385852
hg195852
hg185852
hg175852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7640
Supporting Variants
SamplesNA12878
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)nssv3915
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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