A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6556893



Internal ID9766674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124923260..124924034hg38UCSC Ensembl
chr10:126611829..126612603hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678365
Supporting Variants
SamplesNA19723
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6556893
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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