A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608400



Internal ID6995330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26311176..26311727hg38UCSC Ensembl
Innerchr6:26311206..26311698hg38UCSC Ensembl
Outerchr6:26311147..26311757hg38UCSC Ensembl
chr6:26311404..26311955hg19UCSC Ensembl
Innerchr6:26311434..26311926hg19UCSC Ensembl
Outerchr6:26311375..26311985hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12232693
SamplesHG04152
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608400
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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