A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26271



Internal ID15828232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:26120643..26121022hg38UCSC Ensembl
OuterchrY:26120101..26121315hg38UCSC Ensembl
InnerchrY:28266790..28267169hg19UCSC Ensembl
OuterchrY:28266248..28267462hg19UCSC Ensembl
InnerchrY:26676178..26676557hg18UCSC Ensembl
OuterchrY:26675636..26676850hg18UCSC Ensembl
InnerchrY:26604915..26605294hg17UCSC Ensembl
OuterchrY:26604373..26605587hg17UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg381215
hg191215
hg181215
hg171215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10039
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)nssv26271
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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