A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663797



Internal ID9929902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160581006..160583137hg38UCSC Ensembl
Outerchr6:160580849..160583290hg38UCSC Ensembl
Innerchr6:161002038..161004169hg19UCSC Ensembl
Outerchr6:161001881..161004322hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg382442
hg192442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5799382, essv6588714
SamplesHG00108, HG00256
Known GenesLPA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663797
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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