A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21170



Internal ID15837797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18595008..19631590hg38UCSC Ensembl
Outerchr14:18591020..19635904hg38UCSC Ensembl
Innerchr14:19371485..20099873hg19UCSC Ensembl
Outerchr14:19367497..20104136hg19UCSC Ensembl
Innerchr14:18441485..19169589hg18UCSC Ensembl
Outerchr14:18437497..19173903hg18UCSC Ensembl
Innerchr14:18441485..19169589hg17UCSC Ensembl
Outerchr14:18437497..19173903hg17UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381044885
hg19736640
hg18736407
hg17736407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9117
Supporting Variants
SamplesNA18853
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, POTEG, POTEM
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)nssv21170
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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