A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5899551



Internal ID9371874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31240955..31317962hg38UCSC Ensembl
Outerchr6:31240921..31317997hg38UCSC Ensembl
Innerchr6:31208732..31285739hg19UCSC Ensembl
Outerchr6:31208698..31285774hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3877077
hg1977077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674481
Supporting Variants
SamplesNA18564
Known GenesHLA-C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5899551
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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