A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661882



Internal ID9581301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11914188..12871713hg38UCSC Ensembl
chr3:11955662..12913212hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg38957526
hg19957551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv850e199
Supporting Variantsessv5958685
SamplesNA18538
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)esv2661882
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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