A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609729



Internal ID6996649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81037630..81056079hg38UCSC Ensembl
Innerchr6:81037634..81056076hg38UCSC Ensembl
Outerchr6:81037627..81056083hg38UCSC Ensembl
chr6:81747347..81765796hg19UCSC Ensembl
Innerchr6:81747351..81765793hg19UCSC Ensembl
Outerchr6:81747344..81765800hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3818450
hg1918450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12450960
SamplesHG04177
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609729
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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