A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1328e199



Internal ID22759101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15157199..15159774hg38UCSC Ensembl
chr9:15157197..15159772hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382576
hg192576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658218, esv2673618, esv2676449
SamplesNA19397, HG01188, NA19393, NA18504, NA19190, NA19374, NA19384, NA19371, NA19207, NA19901, NA19189, NA20342, NA18867, HG01124, NA18934, NA19462, NA19982, NA18910, NA20344, HG01390, NA19256, NA18517, NA20276, NA19835, NA19360, NA18501, NA19468, NA19430, NA18505
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1328e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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