A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22255



Internal ID15840662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28318698..28325328hg38UCSC Ensembl
Outerchr15:28318153..28326018hg38UCSC Ensembl
Innerchr15:28563844..28570474hg19UCSC Ensembl
Outerchr15:28563299..28571164hg19UCSC Ensembl
Innerchr15:26237439..26244069hg18UCSC Ensembl
Outerchr15:26236894..26244759hg18UCSC Ensembl
Innerchr15:26237439..26244069hg17UCSC Ensembl
Outerchr15:26236894..26244759hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg387866
hg197866
hg187866
hg177866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9208
Supporting Variants
SamplesNA18980
Known GenesHERC2
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)nssv22255
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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