A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676449



Internal ID9942554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15157712..15159774hg38UCSC Ensembl
chr9:15157710..15159772hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382063
hg192063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1328e199
Supporting Variantsessv6536052, essv5810965, essv5569383, essv5537290, essv5525559, essv6209266, essv5900037, essv6293092, essv6102837, essv6215944, essv6534512, essv5970108, essv6118828, essv6001101, essv5721971, essv6210300, essv6011457, essv6524796, essv6255035, essv5466480, essv5447617, essv6409913, essv5580834, essv6205644, essv5854123
SamplesNA19397, HG01188, NA19393, NA18504, NA19190, NA19207, NA19901, NA19189, NA20342, NA18867, HG01124, NA18934, 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)esv2676449
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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