A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13063



Internal ID15833309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15720913..15721878hg38UCSC Ensembl
Outerchr4:15719720..15722959hg38UCSC Ensembl
Innerchr4:15722536..15723501hg19UCSC Ensembl
Outerchr4:15721343..15724582hg19UCSC Ensembl
Innerchr4:15331634..15332599hg18UCSC Ensembl
Outerchr4:15330441..15333680hg18UCSC Ensembl
Innerchr4:15398805..15399770hg17UCSC Ensembl
Outerchr4:15397612..15400851hg17UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg383240
hg193240
hg183240
hg173240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10459
Supporting Variants
SamplesNA18504
Known GenesBST1
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)nssv13063
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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