A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469602



Internal ID15534317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:26032877..26176673hg38UCSC Ensembl
InnerchrY:28179024..28322820hg19UCSC Ensembl
InnerchrY:26588412..26732208hg18UCSC Ensembl
InnerchrY:27102022..27245818hg16UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38143797
hg19143797
hg18143797
hg16143797
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673085, nssv1673564, nssv1676120, nssv1674427
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)nsv469602
Frequency
Sample Size265
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer