A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611203



Internal ID6998114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149088158..149089267hg38UCSC Ensembl
Innerchr6:149088208..149089217hg38UCSC Ensembl
Outerchr6:149088089..149089336hg38UCSC Ensembl
chr6:149409294..149410403hg19UCSC Ensembl
Innerchr6:149409344..149410353hg19UCSC Ensembl
Outerchr6:149409225..149410472hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12580791, essv12580799, essv12580801, essv12580798, essv12580797, essv12580804, essv12580803, essv12580793, essv12580796, essv12580802, essv12580792, essv12580794, essv12580795, essv12580800
SamplesHG02610, HG01443, NA19020, NA18510, HG03045, HG02570, HG03388, HG03024, HG02675, NA19017, HG02613, HG02558, HG02284, NA19153
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611203
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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