A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673085



Internal ID15530593
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
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469602
Supporting Variants
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)nssv1673085
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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