A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22537



Internal ID15829847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22085403..22188196hg38UCSC Ensembl
Outerchr15:22084356..22192569hg38UCSC Ensembl
Innerchr15:22373354..22476147hg19UCSC Ensembl
Outerchr15:22372307..22480520hg19UCSC Ensembl
Innerchr15:19874718..19977511hg18UCSC Ensembl
Outerchr15:19873671..19981884hg18UCSC Ensembl
Innerchr15:19874718..19977511hg17UCSC Ensembl
Outerchr15:19873671..19981884hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38108214
hg19108214
hg18108214
hg17108214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA11830
Known GenesOR4N3P, OR4N4
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)nssv22537
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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