A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469884



Internal ID15187913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:23593823..23786225hg38UCSC Ensembl
InnerchrY:25739970..25932372hg19UCSC Ensembl
InnerchrY:24149358..24341760hg18UCSC Ensembl
InnerchrY:24585156..24777558hg16UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38192403
hg19192403
hg18192403
hg16192403
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672564, nssv1673985, nssv1672382, nssv1675023, nssv1674769, nssv1675748
Samples
Known Genes
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nsv469884
Frequency
Sample Size265
Observed Gain3
Observed Loss3
Observed Complex0
Frequencyn/a


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