A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6449



Internal ID15190729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:14531333..14563740hg38UCSC Ensembl
Outerchr11:14552879..14585286hg19UCSC Ensembl
Outerchr11:14509455..14541862hg18UCSC Ensembl
Outerchr11:14509455..14541862hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg387026
hg197026
hg187026
hg177026
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7685
Supporting Variants
SamplesNA12156
Known GenesPSMA1
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)nssv6449
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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