A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6401067



Internal ID9378470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28275775..28283753hg38UCSC Ensembl
Outerchr10:28275618..28283906hg38UCSC Ensembl
Innerchr10:28564704..28572682hg19UCSC Ensembl
Outerchr10:28564547..28572835hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388289
hg198289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661194
Supporting Variants
SamplesNA18489
Known GenesMPP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6401067
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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