A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2311e212



Internal ID22785238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77101383..77148083hg38UCSC Ensembl
chrX:76321796..76368537hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3846701
hg1946742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3574070, esv3574074, esv3574084, esv3574069, esv3574081, esv3574077
Samples400287BP, 401110GJ, 400880TM, 400569WC, 400105BB, 401986LC, 401036WS, 401931JL, 400899NK, 400641WJ, 401253MC, 401281BP, 401792KR, 401687LR, 400600DP, 400526DR, 400032RC, 401746WW, 401655DC, 400870KC, 401274PA, 401617KM, 401432SB, 400768MN, 401357MH, 401822TL, 400043HC, 401587RC, 401391PJ, 401428LD, 401016IT, 401315HK, 401268PS, 401149VA, 402073LQ, 401372RR, 401735LE, 401284NA, 400178RH, 400532MH
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)dgv2311e212
Frequency
Sample Size873
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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