A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24708



Internal ID15833023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19742968..19825974hg38UCSC Ensembl
Outerchr14:19742473..19826653hg38UCSC Ensembl
Innerchr14:20211127..20294133hg19UCSC Ensembl
Outerchr14:20210632..20294812hg19UCSC Ensembl
Innerchr14:19280967..19363973hg18UCSC Ensembl
Outerchr14:19280472..19364652hg18UCSC Ensembl
Innerchr14:19280967..19363973hg17UCSC Ensembl
Outerchr14:19280472..19364652hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3884181
hg1984181
hg1884181
hg1784181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9117
Supporting Variants
SamplesNA18502
Known GenesOR4M1, OR4Q3
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)nssv24708
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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