A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5475023



Internal ID9764819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:87576072..87576515hg38UCSC Ensembl
Outerchr6:87576025..87576566hg38UCSC Ensembl
Innerchr6:88285790..88286233hg19UCSC Ensembl
Outerchr6:88285743..88286284hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658829
Supporting Variants
SamplesNA19720
Known GenesRARS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5475023
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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