A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5882896



Internal ID9381161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152835275..152853315hg38UCSC Ensembl
Outerchr6:152835238..152853365hg38UCSC Ensembl
Innerchr6:153156410..153174450hg19UCSC Ensembl
Outerchr6:153156373..153174500hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3818128
hg1918128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664679
Supporting Variants
SamplesNA18573
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5882896
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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