A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12309110



Internal ID3429199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33160090..33160652hg38UCSC Ensembl
Innerchr6:33160098..33160645hg38UCSC Ensembl
Outerchr6:33160083..33160660hg38UCSC Ensembl
chr6:33127867..33128429hg19UCSC Ensembl
Innerchr6:33127875..33128422hg19UCSC Ensembl
Outerchr6:33127860..33128437hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608624
Supporting Variants
SamplesHG03064
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12309110
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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