A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611272



Internal ID6651491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151732227..151739491hg38UCSC Ensembl
Innerchr6:151732267..151739451hg38UCSC Ensembl
Outerchr6:151732187..151739531hg38UCSC Ensembl
chr6:152053362..152060626hg19UCSC Ensembl
Innerchr6:152053402..152060586hg19UCSC Ensembl
Outerchr6:152053322..152060666hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg387265
hg197265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12585001, essv12585002, essv12585004, essv12585003
SamplesHG03941, NA20885, NA20282, HG03902
Known GenesESR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611272
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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