A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607855



Internal ID6648094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:476742..487527hg38UCSC Ensembl
Innerchr6:476742..487527hg38UCSC Ensembl
Outerchr6:476555..487789hg38UCSC Ensembl
chr6:476742..487527hg19UCSC Ensembl
Innerchr6:476742..487527hg19UCSC Ensembl
Outerchr6:476555..487789hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3810786
hg1910786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12169567, essv12169566
SamplesHG03717, HG03917
Known GenesEXOC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607855
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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