A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1402e199



Internal ID22759175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140411591..140420873hg38UCSC Ensembl
chrX:139493756..139503038hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg389283
hg199283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2668442, esv2676956
SamplesNA12889, NA19657, HG01171, NA20524, HG00275, NA19654, NA19436, NA19434, HG00278, NA20803, NA19713, HG00595, HG01191
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1402e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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