A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv345e199



Internal ID22758118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33558308..33565455hg38UCSC Ensembl
chr13:34132445..34139592hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg387148
hg197148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2670631, esv2657576
SamplesNA19703, NA19397, NA19359, NA20356, NA19920, NA19374, NA19457, NA20287, NA20291, NA19651, NA19385, NA19901, NA20342, NA19985, NA19908, NA19462, NA19236, NA19982, NA19452, NA19469, NA19435, NA19470, NA19467, NA20341, NA19818, NA20348, NA19713, NA20289, NA19900
Known GenesSTARD13
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv345e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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