A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22775



Internal ID15830789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384746..20421378hg38UCSC Ensembl
Outerchr15:20383459..20427491hg38UCSC Ensembl
Innerchr15:20589999..20626631hg19UCSC Ensembl
Outerchr15:20588712..20632744hg19UCSC Ensembl
Innerchr15:18850013..18886645hg18UCSC Ensembl
Outerchr15:18848726..18892758hg18UCSC Ensembl
Innerchr15:18850013..18886645hg17UCSC Ensembl
Outerchr15:18848726..18892758hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3844033
hg1944033
hg1844033
hg1744033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12155
Known GenesHERC2P3
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)nssv22775
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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