A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23280



Internal ID15842234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22015979..22017226hg38UCSC Ensembl
Outerchr15:22015551..22018282hg38UCSC Ensembl
Innerchr15:22303930..22305177hg19UCSC Ensembl
Outerchr15:22303502..22306233hg19UCSC Ensembl
Innerchr15:19805294..19806541hg18UCSC Ensembl
Outerchr15:19804866..19807597hg18UCSC Ensembl
Innerchr15:19805294..19806541hg17UCSC Ensembl
Outerchr15:19804866..19807597hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382732
hg192732
hg182732
hg172732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA19144
Known GenesLOC727924
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)nssv23280
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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