A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469704



Internal ID15187733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72377033..72561586hg38UCSC Ensembl
Innerchr15:72669374..72853927hg19UCSC Ensembl
Innerchr15:70456428..70640981hg18UCSC Ensembl
Innerchr15:70385192..70569745hg16UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38184554
hg19184554
hg18184554
hg16184554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673946, nssv1676130, nssv1675397
Samples
Known GenesARIH1, HEXA-AS1, TMEM202
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)nsv469704
Frequency
Sample Size265
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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