A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15364



Internal ID15481795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39875..69635hg38UCSC Ensembl
Outerchr7:39359..70666hg38UCSC Ensembl
Innerchr7:39875..69635hg19UCSC Ensembl
Outerchr7:39359..70666hg19UCSC Ensembl
Innerchr7:134958..164718hg18UCSC Ensembl
Outerchr7:134442..165749hg18UCSC Ensembl
Innerchr7:134958..164718hg17UCSC Ensembl
Outerchr7:134442..165749hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3831308
hg1931308
hg1831308
hg1731308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8023
Supporting Variants
SamplesNA10839
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv15364
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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