A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609266



Internal ID6649497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63747755..63751139hg38UCSC Ensembl
Innerchr6:63747776..63751119hg38UCSC Ensembl
Outerchr6:63747735..63751160hg38UCSC Ensembl
chr6:64457648..64461032hg19UCSC Ensembl
Innerchr6:64457669..64461012hg19UCSC Ensembl
Outerchr6:64457628..64461053hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg383385
hg193385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12389856
SamplesHG02274
Known GenesEYS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609266
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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