A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661565



Internal ID9927670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44313195..44315118hg38UCSC Ensembl
chr10:44808643..44810566hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381924
hg191924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6126860, essv6377184, essv6325945, essv6133094, essv5504461, essv5494979, essv5437903
SamplesHG01173, NA07347, HG00311, HG00323, NA06989, HG00280, HG00343
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661565
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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