A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25738



Internal ID15836849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15877101..15877103hg38UCSC Ensembl
Outerchr22:15876951..15877205hg38UCSC Ensembl
Innerchr22:16100860..16100862hg19UCSC Ensembl
Outerchr22:16100758..16101012hg19UCSC Ensembl
Innerchr22:14480860..14480862hg18UCSC Ensembl
Outerchr22:14480758..14481012hg18UCSC Ensembl
Innerchr22:14480860..14480862hg17UCSC Ensembl
Outerchr22:14480758..14481012hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38255
hg19255
hg18255
hg17255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9866
Supporting Variants
SamplesNA18564
Known Genes
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)nssv25738
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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