A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10796



Internal ID15845759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:60001..126418hg38UCSC Ensembl
Outerchr6:60001..126418hg19UCSC Ensembl
Outerchr6:5001..71418hg18UCSC Ensembl
Outerchr6:1..71418hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3866418
hg1966418
hg1866418
hg1771418
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16470, nssv15001, nssv13965, nssv13150, nssv14496, nssv14374, nssv15831, nssv15861, nssv13884, nssv14158, nssv12829, nssv15807, nssv15673, nssv13892, nssv13880, nssv15703
SamplesNA07029, NA18504, NA12802, NA18860, NA10839, NA18975, NA10863, NA18572, NA19221, NA18537, NA18853, NA19132, NA19240, NA19144
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)nsv10796
Frequency
Sample Size31
Observed Gain11
Observed Loss3
Observed Complex0
Frequencyn/a


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