A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1666e212



Internal ID20150122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169299082..169309286hg38UCSC Ensembl
chr5:168726086..168736290hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3810205
hg1910205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3570547, esv3570548, esv3570546
Samples401459HF, 400308SP, 401366WD, 400424LN, 400268SY, 401489CB, 401052BM, 401146US, 400554WB, 400889CM, 401592NR, 400512LR, 400574MA, 401384BP, 401195PN, 401721CP, 401093VL, 401355CD, 400620MT, 400523GB, 401258PC, 401975VD, 400606HW, 401860TJ, 400482MD, 401263HS, 401908YM, 400022WA, 401538NS, 400749VW, 400292LP, 400427SD, 400385LJ, 400353ML, 401234MB, 400198MD, 400383HL, 401785MJ, 400352CA, 400038CK, 401331LJ, 400825TW, 401900RJ, 401870FB, 401499JR, 400040CN, 400070PC, 402033WD, 400702PA, 401913GT, 402052ZA, 401357MH, 401454CD, 401348RB, 401519SA, 400082SD, 401475MK, 401730MS, 401506LK, 401943KA, 4000657TM, 400800MW, 401619BT, 401504RJ, 400171BJ, 402022SM, 400387HE, 400639RP, 401889FR, 400603CJ, 401875FG, 400278PD, 400014SL, 401369GR, 401176BD, 400474GF, 401514BA, 401922MW, 400177CG, 401361GG, 400601WC, 400376SJ, 400295PS, 401025SM, 401012TP, 401413RG, 400586RD, 401567BD, 401152MV, 400930MK, 400323AA, 401372RR, 401135CS, 400106PC, 401266HM, 400108BJ, 400261RN, 400581VJ, 400291VJ, 401053MF, 400209BS, 402024BB, 401480PG, 400890IT, 400152MR, 400234CA, 401246HH, 400782IE, 401207DA
Known GenesSLIT3
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)dgv1666e212
Frequency
Sample Size873
Observed Gain0
Observed Loss109
Observed Complex0
Frequencyn/a


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