A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10592



Internal ID15845555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:157401231..157409113hg38UCSC Ensembl
Outerchr4:158322383..158330265hg19UCSC Ensembl
Outerchr4:158541833..158549715hg18UCSC Ensembl
Outerchr4:158679988..158687870hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg387883
hg197883
hg187883
hg177883
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13731, nssv12316
SamplesNA18860, NA18552
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)nsv10592
Frequency
Sample Size31
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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