A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611273



Internal ID6651492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151882689..151887701hg38UCSC Ensembl
Innerchr6:151882689..151887701hg38UCSC Ensembl
Outerchr6:151882375..151887918hg38UCSC Ensembl
chr6:152203824..152208836hg19UCSC Ensembl
Innerchr6:152203824..152208836hg19UCSC Ensembl
Outerchr6:152203510..152209053hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg385013
hg195013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12585006, essv12585005
SamplesNA20859, NA20849
Known GenesESR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611273
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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