A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26044



Internal ID15491906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28947826..28948627hg38UCSC Ensembl
Outerchr15:28947412..28949055hg38UCSC Ensembl
Innerchr15:29240029..29240830hg19UCSC Ensembl
Outerchr15:29239615..29241258hg19UCSC Ensembl
Innerchr15:27027321..27028122hg18UCSC Ensembl
Outerchr15:27026907..27028550hg18UCSC Ensembl
Innerchr15:27027321..27028122hg17UCSC Ensembl
Outerchr15:27026907..27028550hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381644
hg191644
hg181644
hg171644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9224
Supporting Variants
SamplesNA18860
Known GenesAPBA2
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)nssv26044
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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