A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6015477



Internal ID8992880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28143578..28143877hg38UCSC Ensembl
chr10:28432507..28432806hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672420
Supporting Variants
SamplesHG00108
Known GenesMPP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6015477
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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