A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6126860



Internal ID9104263
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 Flag1
Merged StatusS
Merged Variantsesv2661565
Supporting Variants
SamplesHG00323
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6126860
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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