A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15818



Internal ID15830548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160606460..160607818hg38UCSC Ensembl
Outerchr6:160606022..160609055hg38UCSC Ensembl
Innerchr6:161027492..161028850hg19UCSC Ensembl
Outerchr6:161027054..161030087hg19UCSC Ensembl
Innerchr6:160947482..160948840hg18UCSC Ensembl
Outerchr6:160947044..160950077hg18UCSC Ensembl
Innerchr6:160997903..160999261hg17UCSC Ensembl
Outerchr6:160997465..161000498hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg383034
hg193034
hg183034
hg173034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7986
Supporting Variants
SamplesNA12155
Known GenesLPA
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)nssv15818
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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