A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607921



Internal ID6648160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3070363..3072626hg38UCSC Ensembl
Innerchr6:3070363..3072626hg38UCSC Ensembl
Outerchr6:3070065..3072879hg38UCSC Ensembl
chr6:3070597..3072860hg19UCSC Ensembl
Innerchr6:3070597..3072860hg19UCSC Ensembl
Outerchr6:3070299..3073113hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382264
hg192264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12178832, essv12178835, essv12178834, essv12178833
SamplesNA18605, HG02142, HG00708, NA18536
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607921
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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