A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12454264



Internal ID2744399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84815325..84828493hg38UCSC Ensembl
Innerchr6:84815825..84827993hg38UCSC Ensembl
Outerchr6:84814325..84829493hg38UCSC Ensembl
chr6:85525043..85538211hg19UCSC Ensembl
Innerchr6:85525543..85537711hg19UCSC Ensembl
Outerchr6:85524043..85539211hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3813169
hg1913169
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609803
Supporting Variants
SamplesHG02409
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12454264
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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