A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667428



Internal ID9933533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42801161..42801318hg38UCSC Ensembl
chr15:43093359..43093516hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5842879, essv6307875, essv5651677, essv5738661, essv6487537, essv6588186, essv6174021, essv5830527, essv6121791, essv6461706, essv5867798, essv5971793, essv6206323, essv5804967, essv5479413, essv6529538, essv5834608, essv6067943, essv5423693, essv6030495, essv6539865, essv5455432, essv6435426, essv5724883, essv5627087, essv5991295, essv5740243, essv5685801, essv6230487, essv6440759, essv6504398, essv5410250, essv5606397, essv5970438, essv5580014
SamplesNA20766, NA11829, NA19704, NA11931, HG00315, HG00640, HG00271, NA20537, NA20589, HG01354, HG01083, NA20513, HG00158, HG00139, NA11994, NA18520, HG00739, NA11993, HG00260, NA12489, HG00268, HG00282, HG00732, NA20536, NA20519, HG00740, NA19675, HG00136, HG00319, NA12830, NA20503, NA19755, NA12006, NA12154, NA18620
Known GenesTTBK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667428
Frequency
Sample Size1151
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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