A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607940



Internal ID6994871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4013852..4015432hg38UCSC Ensembl
Innerchr6:4013902..4015382hg38UCSC Ensembl
Outerchr6:4013802..4015482hg38UCSC Ensembl
chr6:4014086..4015666hg19UCSC Ensembl
Innerchr6:4014136..4015616hg19UCSC Ensembl
Outerchr6:4014036..4015716hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381581
hg191581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12179408, essv12179407, essv12179406, essv12179410, essv12179409
SamplesHG03280, NA19319, HG02756, HG03446, HG03063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607940
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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