A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669



Internal ID15550501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:25023585..25054511hg38UCSC Ensembl
Outerchr7:25063204..25094130hg19UCSC Ensembl
Outerchr7:25029729..25060655hg18UCSC Ensembl
Outerchr7:24836444..24867370hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg388822
hg198822
hg188822
hg178822
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513
SamplesNA12878
Known Genes
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)nsv5669
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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