A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7983



Internal ID15845895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:159664365..159668795hg38UCSC Ensembl
Outerchr6:160085397..160089827hg19UCSC Ensembl
Outerchr6:160005387..160009817hg18UCSC Ensembl
Outerchr6:160055808..160060238hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384431
hg194431
hg184431
hg174431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15034, nssv15048, nssv17183, nssv14364, nssv15256, nssv17474, nssv16332, nssv14525, nssv14797, nssv13639, nssv14835
SamplesNA18502, NA11830, NA10839, NA18975, NA10847, NA18572, NA18537, NA18517, NA18564, NA18972, 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)nsv7983
Frequency
Sample Size31
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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