A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609593



Internal ID6996514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76107127..76115227hg38UCSC Ensembl
Innerchr6:76107127..76115227hg38UCSC Ensembl
Outerchr6:76106627..76115727hg38UCSC Ensembl
chr6:76816844..76824944hg19UCSC Ensembl
Innerchr6:76816844..76824944hg19UCSC Ensembl
Outerchr6:76816344..76825444hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg388101
hg198101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12430770, essv12430768, essv12430771, essv12430767, essv12430769
SamplesNA19909, NA18565, NA18988, NA19317, NA18984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609593
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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