A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27792



Internal ID15833228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:6245572..6249718hg38UCSC Ensembl
OuterchrY:6244587..6250093hg38UCSC Ensembl
InnerchrY:6113613..6117759hg19UCSC Ensembl
OuterchrY:6112628..6118134hg19UCSC Ensembl
InnerchrY:6173613..6177759hg18UCSC Ensembl
OuterchrY:6172628..6178134hg18UCSC Ensembl
InnerchrY:6156974..6161120hg17UCSC Ensembl
OuterchrY:6155989..6161495hg17UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg385507
hg195507
hg185507
hg175507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10012
Supporting Variants
SamplesNA18504
Known GenesTSPY2
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)nssv27792
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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