A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19035



Internal ID15834719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47456492..47481148hg38UCSC Ensembl
Outerchr10:47455951..47481159hg38UCSC Ensembl
Innerchr10:48258214..48282870hg19UCSC Ensembl
Outerchr10:48258203..48283411hg19UCSC Ensembl
Innerchr10:47878220..47902876hg18UCSC Ensembl
Outerchr10:47878209..47903417hg18UCSC Ensembl
Innerchr10:47878220..47902876hg17UCSC Ensembl
Outerchr10:47878209..47903417hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3825209
hg1925209
hg1825209
hg1725209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18537
Known GenesANXA8
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)nssv19035
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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