A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv642e199



Internal ID22758415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40838625..40869922hg38UCSC Ensembl
chr19:41344530..41375827hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3831298
hg1931298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2676382, esv2676981, esv2677447
SamplesHG01060, HG01356, HG00361, NA19066, HG00242, HG00559, NA18507, HG01389, HG01066, NA18603, HG00367, HG00318, HG00181, NA19819, NA12340, HG01456, NA18606, NA18616, NA19443, HG00693, HG00501, NA19382, NA19315, NA20769, HG00270, NA20336, NA19404, HG01134, HG01069, HG00325, HG00422, NA19725, NA19921, HG00464, HG01136, NA18605, NA19247, NA19657, NA19056, HG00328, HG00732, HG00577, NA19455, HG00436, HG00583, HG01390, HG00651, HG00613, NA20282, NA19059, NA19469, NA18945, NA18541, NA19652, NA19440, NA19834, NA18543, NA18628, HG00734, NA19835, NA19324, NA19083, NA18943, HG00662, NA19085, NA18615, HG00620, HG00269, HG00707, HG00672, HG00578, NA19472, NA19713, HG00186, HG00698, HG00280, NA19080, NA19711, HG00377, NA18989, NA19004, NA18488, HG00628, HG01191, NA18622, HG00581, NA19676
Known GenesCYP2A6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv642e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss87
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer