A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9752



Internal ID15847664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54218894..54244649hg38UCSC Ensembl
Outerchr19:54722763..54748490hg19UCSC Ensembl
Outerchr19:59414575..59440302hg18UCSC Ensembl
Outerchr19:59414575..59440302hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3825756
hg1925728
hg1825728
hg1725728
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22181, nssv25554, nssv24972, nssv28601, nssv27642, nssv24624, nssv25390, nssv25376, nssv27852, nssv25939, nssv26010, nssv27051, nssv27590, nssv24693, nssv25472, nssv25990, nssv27071, nssv27475, nssv27061, nssv28570, nssv27598, nssv21815
SamplesNA18502, NA11830, NA18980, NA18504, NA18860, NA07048, NA10839, NA18975, NA10847, NA12872, NA19221, NA18853, NA19132, NA18517, NA18564, NA19173
Known GenesLILRA6, LILRB3
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)nsv9752
Frequency
Sample Size31
Observed Gain10
Observed Loss6
Observed Complex0
Frequencyn/a


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