A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1104e199



Internal ID22758877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32510927..32549678hg38UCSC Ensembl
chr6:32478704..32517455hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3838752
hg1938752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672813, esv2660994
SamplesNA19394, NA12717, NA11830, NA18508, HG01359, NA19399, NA18980, NA18507, NA20816, NA18486, NA19393, HG00449, HG00177, NA19190, HG00337, HG00327, NA20814, NA20796, NA19379, NA18944, HG00448, NA20795, NA20769, NA18547, NA18942, NA20768, NA18498, NA20541, HG00281, NA12275, NA19383, HG00335, NA20819, HG00325, NA12044, HG01259, HG00427, NA20811, NA19189, HG00338, NA18973, HG00419, NA19921, HG00133, HG01136, NA18605, NA18613, HG01187, NA19391, NA18516, NA20506, NA18579, NA18566, HG00284, HG00273, NA12829, HG00321, NA19225, NA20828, NA18523, NA18536, NA19625, NA20765, HG00258, NA20773, NA19390, NA19147, NA18559, NA18517, NA12775, NA20804, HG00278, NA20520, NA20530, NA20778, NA19470, NA19428, NA20544, NA19467, HG00116, NA20516, NA19360, NA19398, NA18501, HG00656, NA19713, NA19129, HG00345, NA20585, NA18522, NA19431
Known GenesHLA-DRB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1104e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss91
Observed Complex0
Frequencyn/a


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