A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610266



Internal ID6650492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106112750..106457586hg38UCSC Ensembl
Innerchr6:106112900..106457436hg38UCSC Ensembl
Outerchr6:106112600..106457736hg38UCSC Ensembl
chr6:106560625..106905461hg19UCSC Ensembl
Innerchr6:106560775..106905311hg19UCSC Ensembl
Outerchr6:106560475..106905611hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38344837
hg19344837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12498601
SamplesHG03063
Known GenesATG5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610266
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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