A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26129



Internal ID15828055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21939800..21940179hg38UCSC Ensembl
OuterchrY:21939507..21940722hg38UCSC Ensembl
InnerchrY:24085947..24086326hg19UCSC Ensembl
OuterchrY:24085654..24086869hg19UCSC Ensembl
InnerchrY:22495335..22495714hg18UCSC Ensembl
OuterchrY:22495042..22496257hg18UCSC Ensembl
InnerchrY:22424072..22424451hg17UCSC Ensembl
OuterchrY:22423779..22424994hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg381216
hg191216
hg181216
hg171216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10028
Supporting Variants
SamplesNA07048
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)nssv26129
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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