A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610293



Internal ID6997210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107207864..107209752hg38UCSC Ensembl
Innerchr6:107207877..107209739hg38UCSC Ensembl
Outerchr6:107207851..107209765hg38UCSC Ensembl
chr6:107529068..107530956hg19UCSC Ensembl
Innerchr6:107529081..107530943hg19UCSC Ensembl
Outerchr6:107529055..107530969hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381889
hg191889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12499103, essv12499096, essv12499102, essv12499105, essv12499100, essv12499104, essv12499106, essv12499097, essv12499099, essv12499098, essv12499101, essv12499095
SamplesHG00881, HG03736, HG03209, NA19451, HG02364, NA19320, NA19452, HG00864, HG02371, HG01028, HG01799, HG00759
Known GenesPDSS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610293
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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