A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26987



Internal ID15844169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21071593..21072383hg38UCSC Ensembl
Outerchr15:21070902..21072825hg38UCSC Ensembl
Innerchr15:21276922..21277712hg19UCSC Ensembl
Outerchr15:21276231..21278154hg19UCSC Ensembl
Innerchr15:19541581..19542371hg18UCSC Ensembl
Outerchr15:19540890..19542813hg18UCSC Ensembl
Innerchr15:19541581..19542371hg17UCSC Ensembl
Outerchr15:19540890..19542813hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381924
hg191924
hg181924
hg171924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA19221
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)nssv26987
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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