A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15622



Internal ID15839166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153786819..154111254hg38UCSC Ensembl
Outerchr7:153786053..154111761hg38UCSC Ensembl
Innerchr7:153483904..153808339hg19UCSC Ensembl
Outerchr7:153483138..153808846hg19UCSC Ensembl
Innerchr7:153114837..153439272hg18UCSC Ensembl
Outerchr7:153114071..153439779hg18UCSC Ensembl
Innerchr7:152921552..153245987hg17UCSC Ensembl
Outerchr7:152920786..153246494hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38325709
hg19325709
hg18325709
hg17325709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8237
Supporting Variants
SamplesNA18942
Known GenesDPP6
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)nssv15622
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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