A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22557



Internal ID15841902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3247708..3337972hg38UCSC Ensembl
Outerchr11:3235394..3338635hg38UCSC Ensembl
Innerchr11:3268938..3359202hg19UCSC Ensembl
Outerchr11:3256624..3359865hg19UCSC Ensembl
Innerchr11:3225514..3315778hg18UCSC Ensembl
Outerchr11:3213200..3316441hg18UCSC Ensembl
Innerchr11:3225514..3315778hg17UCSC Ensembl
Outerchr11:3213200..3316441hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38103242
hg19103242
hg18103242
hg17103242
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8770
Supporting Variants
SamplesNA19132
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)nssv22557
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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