A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611563



Internal ID6651781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162637236..162641487hg38UCSC Ensembl
Innerchr6:162637237..162641486hg38UCSC Ensembl
Outerchr6:162637235..162641488hg38UCSC Ensembl
chr6:163058268..163062519hg19UCSC Ensembl
Innerchr6:163058269..163062518hg19UCSC Ensembl
Outerchr6:163058267..163062520hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg384252
hg194252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12621770, essv12621774, essv12621768, essv12621778, essv12621772, essv12621773, essv12621777, essv12621775, essv12621769, essv12621776, essv12621771
SamplesNA20887, HG02272, HG03019, HG02789, HG02778, HG02775, HG01620, HG04227, HG03660, HG03743, HG03009
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611563
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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