A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673985



Internal ID15184807
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 loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469884
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)nssv1673985
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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