A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665684



Internal ID9931789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:101170467..101196332hg38UCSC Ensembl
Outerchr6:101170310..101196485hg38UCSC Ensembl
Innerchr6:101618343..101644208hg19UCSC Ensembl
Outerchr6:101618186..101644361hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3826176
hg1926176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6040201, essv5586256
SamplesHG00577, HG00584
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665684
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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