A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2243e212



Internal ID22785170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26022260..26036829hg38UCSC Ensembl
chrX:26040377..26054946hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3814570
hg1914570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3573692, esv3573693
Samples400364SS, 400634MP, 401734PG, 400094RS, 400658BW, 401019MP, 401808PS, 402064DC, 401687LR, 402065BG, 401184MM, 400817MB, 400609FJ, 401732HW, 400110MD, 401423BA, 401262RR, 401086MD, 400598DA, 400135DR, 400671PP, 401567BD, 400508RD, 401969DR, 400234CA
Known Genes
MethodSNP array
AnalysisWe used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection.
PlatformAffymetrix CytoScan HD 2.7M array
Comments
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)dgv2243e212
Frequency
Sample Size873
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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