A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5784037



Internal ID8761440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30034491..30043476hg38UCSC Ensembl
chr10:30323420..30332405hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg388986
hg198986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672894
Supporting Variants
SamplesNA12830
Known GenesKIAA1462
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5784037
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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