A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19789



Internal ID15837217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23810807..23816058hg38UCSC Ensembl
Outerchr15:23810219..23840455hg38UCSC Ensembl
Innerchr15:24055954..24061205hg19UCSC Ensembl
Outerchr15:24055366..24085602hg19UCSC Ensembl
Innerchr15:21607047..21612298hg18UCSC Ensembl
Outerchr15:21606459..21636695hg18UCSC Ensembl
Innerchr15:21607047..21612298hg17UCSC Ensembl
Outerchr15:21606459..21636695hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3830237
hg1930237
hg1830237
hg1730237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9193
Supporting Variants
SamplesNA18572
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)nssv19789
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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