A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19210



Internal ID15831882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22028343..22043667hg38UCSC Ensembl
Outerchr15:22022701..22044255hg38UCSC Ensembl
Innerchr15:22316294..22331618hg19UCSC Ensembl
Outerchr15:22310652..22332206hg19UCSC Ensembl
Innerchr15:19817658..19832982hg18UCSC Ensembl
Outerchr15:19812016..19833570hg18UCSC Ensembl
Innerchr15:19817658..19832982hg17UCSC Ensembl
Outerchr15:19812016..19833570hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3821555
hg1921555
hg1821555
hg1721555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12802
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)nssv19210
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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