A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608637



Internal ID6995561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33608385..33612177hg38UCSC Ensembl
Innerchr6:33608385..33612177hg38UCSC Ensembl
Outerchr6:33608086..33612476hg38UCSC Ensembl
chr6:33576162..33579954hg19UCSC Ensembl
Innerchr6:33576162..33579954hg19UCSC Ensembl
Outerchr6:33575863..33580253hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg383793
hg193793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12310218, essv12310217
SamplesHG04161, NA18549
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608637
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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