A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15455



Internal ID15482307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144122819..144123930hg38UCSC Ensembl
Outerchr7:144122246..144124639hg38UCSC Ensembl
Innerchr7:143819912..143821023hg19UCSC Ensembl
Outerchr7:143819339..143821732hg19UCSC Ensembl
Innerchr7:143450845..143451956hg18UCSC Ensembl
Outerchr7:143450272..143452665hg18UCSC Ensembl
Innerchr7:143257560..143258671hg17UCSC Ensembl
Outerchr7:143256987..143259380hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg382394
hg192394
hg182394
hg172394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8227
Supporting Variants
SamplesNA10847
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)nssv15455
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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