A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv850e199



Internal ID20124152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11914188..12872013hg38UCSC Ensembl
chr3:11955662..12913512hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg38957826
hg19957851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2677824, esv2661882
SamplesNA18535, NA18960, NA19676, NA18999, NA18538
Known GenesC3orf83, CAND2, MKRN2, PPARG, RAF1, RPL32, SNORA7A, SYN2, TIMP4, TMEM40, TSEN2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv850e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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