A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610341



Internal ID6997258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109855785..109861424hg38UCSC Ensembl
chr6:110176988..110182627hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385640
hg195640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12501110, essv12501115, essv12501108, essv12501117, essv12501113, essv12501120, essv12501112, essv12501114, essv12501118, essv12501109, essv12501119, essv12501111, essv12501107, essv12501116
SamplesNA19141, NA18486, HG03126, NA19068, NA19315, NA19172, HG01440, NA18613, NA18516, NA19000, HG00531, NA19309, HG00136, HG01437
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610341
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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