A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657587



Internal ID9923692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31210140..31210935hg38UCSC Ensembl
chr10:31499069..31499864hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5970973, essv6067667, essv5472759, essv6559567, essv6568532, essv6280388, essv5597857, essv6552639, essv5849331, essv6346561, essv6167380, essv5886539
SamplesNA19466, NA18508, NA18504, NA19381, NA19382, NA19904, HG01101, NA19147, NA19380, HG01342, NA19248, NA19900
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657587
Frequency
Sample Size1151
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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