A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12225819



Internal ID3461330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22911979..22918297hg38UCSC Ensembl
Innerchr6:22911979..22918297hg38UCSC Ensembl
Outerchr6:22911830..22918458hg38UCSC Ensembl
chr6:22912208..22918526hg19UCSC Ensembl
Innerchr6:22912208..22918526hg19UCSC Ensembl
Outerchr6:22912059..22918687hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386319
hg196319
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608342
Supporting Variants
SamplesHG03082
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12225819
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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