A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609882



Internal ID6996801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88358010..88412409hg38UCSC Ensembl
Innerchr6:88358010..88412409hg38UCSC Ensembl
Outerchr6:88357510..88412909hg38UCSC Ensembl
chr6:89067729..89122128hg19UCSC Ensembl
Innerchr6:89067729..89122128hg19UCSC Ensembl
Outerchr6:89067229..89122628hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3854400
hg1954400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12457600
SamplesNA18644
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609882
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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