A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658861



Internal ID9924966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38075800..38075960hg38UCSC Ensembl
chr9:38075797..38075957hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5966809, essv6438643, essv6169325, essv6133016, essv5456721, essv5523910, essv5980283, essv5434743, essv5424413, essv6531300, essv5691182, essv5469413, essv5620458, essv6419190, essv5859993, essv5985779, essv5746946, essv6168879, essv6155402, essv5877359, essv5436482, essv6467102, essv6027233, essv5475349, essv5847324, essv5858097, essv5594429
SamplesHG01060, HG01173, NA18621, HG00249, HG01052, HG00699, HG01051, HG01350, HG00334, HG00537, HG01067, HG00705, HG00464, HG00137, NA18613, HG00320, HG00619, HG01101, HG00140, HG00463, NA18632, HG00111, HG00329, HG00131, HG01082, NA18624, HG00437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658861
Frequency
Sample Size1151
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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