A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6429



Internal ID15537435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:224495..256679hg38UCSC Ensembl
Outerchr11:224495..256679hg19UCSC Ensembl
Outerchr11:214495..246679hg18UCSC Ensembl
Outerchr11:214495..246679hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387251
hg197251
hg187251
hg177251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7632
Supporting Variants
SamplesNA12156
Known GenesPSMD13, SIRT3
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)nssv6429
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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