A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10409



Internal ID15498686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:10005..71427hg38UCSC Ensembl
Outerchr4:10005..71319hg19UCSC Ensembl
Outerchr4:5..61319hg18UCSC Ensembl
Outerchr4:5..61319hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3861423
hg1961315
hg1861315
hg1761315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11677, nssv12501, nssv11707, nssv12612, nssv13620
SamplesNA18860, NA18502, NA19221, NA11830
Known GenesZNF595, ZNF718
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)nsv10409
Frequency
Sample Size31
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer