A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6487004



Internal ID8877146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128890284..128895550hg38UCSC Ensembl
chr10:130688548..130693814hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385267
hg195267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668142
Supporting Variants
SamplesHG00328
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6487004
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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