A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662803



Internal ID9928908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91089132..91090805hg38UCSC Ensembl
Outerchr6:91089095..91090855hg38UCSC Ensembl
Innerchr6:91798850..91800523hg19UCSC Ensembl
Outerchr6:91798813..91800573hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381761
hg191761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6378866
SamplesNA06986
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662803
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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