A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609064



Internal ID6995987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55153613..55165905hg38UCSC Ensembl
Innerchr6:55154113..55165405hg38UCSC Ensembl
Outerchr6:55152613..55166905hg38UCSC Ensembl
chr6:55018411..55030703hg19UCSC Ensembl
Innerchr6:55018911..55030203hg19UCSC Ensembl
Outerchr6:55017411..55031703hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3812293
hg1912293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12361779
SamplesHG02983
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609064
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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