A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24773



Internal ID15495112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73568178..73573597hg38UCSC Ensembl
Outerchr14:73564692..73574863hg38UCSC Ensembl
Innerchr14:74034882..74040301hg19UCSC Ensembl
Outerchr14:74031396..74041567hg19UCSC Ensembl
Innerchr14:73104635..73110054hg18UCSC Ensembl
Outerchr14:73101149..73111320hg18UCSC Ensembl
Innerchr14:73104635..73110054hg17UCSC Ensembl
Outerchr14:73101149..73111320hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3810172
hg1910172
hg1810172
hg1710172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9153
Supporting Variants
SamplesNA19132
Known GenesACOT2
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)nssv24773
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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