A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1070e199



Internal ID22758843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3618945..3621627hg38UCSC Ensembl
chr6:3619179..3621861hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382683
hg192683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2669089, esv2664554
SamplesHG00536, HG00559, HG01374, HG00699, HG00566, NA18602, HG00693, HG00663, NA19660, NA18944, NA18982, NA18635, NA18567, HG00610, NA18574, NA18582, NA19088, NA19681, HG01072, NA19731, HG00422, HG00419, NA18605, NA18613, HG00533, HG00500, NA18566, HG00404, HG00531, HG00479, HG00613, NA18555, NA19685, NA18953, NA18535, NA18961, NA18559, HG00625, NA18628, NA12046, HG01137, NA19085, HG00578, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1070e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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