A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv163e199



Internal ID22757936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93281902..93286063hg38UCSC Ensembl
chr10:95041659..95045820hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg384162
hg194162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2661609, esv2668580
SamplesHG00650, NA18530, NA19067, NA18988, HG00337, NA18558, HG00634, HG00537, NA18977, NA19075, HG00422, NA18990, NA18557, HG00419, HG00543, NA19070, HG00436, NA18637, HG00619, HG00651, NA19655, HG00690, HG00479, NA19009, HG00704, NA18536, NA18634, NA18576, NA18546, NA18543, NA18628, NA18631, NA18987, NA19661, HG00472, HG01125, NA18549, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv163e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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