A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609199



Internal ID6996121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61125347..61184886hg38UCSC Ensembl
chr6:62052828..62112367hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3859540
hg1959540
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12386643, essv12386642, essv12386644, essv12386645, essv12386646
SamplesNA11931, HG00127, NA19717, HG03488, HG02351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609199
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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