A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1152e199



Internal ID22758925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134267107..134274204hg38UCSC Ensembl
chr6:134588245..134595342hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg387098
hg197098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2677003, esv2658663
SamplesHG00626, HG00650, HG00542, HG00442, HG00536, HG00608, NA18621, NA18592, NA18565, NA18561, NA18599, NA18603, NA18530, NA18606, NA18616, HG00654, NA18633, NA18602, HG00663, HG00589, NA18597, NA18595, HG00702, NA18635, NA18619, NA18558, NA18547, NA18618, HG00610, NA18574, NA18582, NA18571, HG00537, HG00590, HG00683, NA18560, HG00534, NA18617, HG00419, NA18539, NA18638, NA18614, HG00543, NA18544, HG00560, NA18605, NA18613, HG00629, NA18538, HG00701, HG00657, HG00556, HG00533, HG00583, HG00500, NA18579, NA18548, NA18537, NA18566, NA18573, NA18626, HG00690, HG00404, HG00531, HG00613, HG00704, NA18593, NA18541, NA18576, NA18608, NA18632, HG00476, NA18542, NA18535, NA18559, HG00625, NA18564, HG00565, HG00662, HG00672, HG00614, HG00513, HG00478, NA18631, HG00421, HG00656, NA18636, NA18609, HG00698, HG00595, NA18624, NA18549, NA18622, NA18562, NA18577, HG00593
Known GenesSGK1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1152e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss96
Observed Complex0
Frequencyn/a


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