A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15069



Internal ID15831418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:292978..295278hg38UCSC Ensembl
Outerchr6:291563..296581hg38UCSC Ensembl
Innerchr6:292978..295278hg19UCSC Ensembl
Outerchr6:291563..296581hg19UCSC Ensembl
Innerchr6:237978..240278hg18UCSC Ensembl
Outerchr6:236563..241581hg18UCSC Ensembl
Innerchr6:237978..240278hg17UCSC Ensembl
Outerchr6:236563..241581hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg385019
hg195019
hg185019
hg175019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10799
Supporting Variants
SamplesNA12740
Known GenesDUSP22
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)nssv15069
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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