A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610009



Internal ID6996928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94356826..94499838hg38UCSC Ensembl
chr6:95066544..95209556hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38143013
hg19143013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1204e214
Supporting Variantsessv12466973, essv12466972, essv12466974
SamplesNA20357, HG03729, NA20289
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610009
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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