A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611528



Internal ID6651746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162373374..162438050hg38UCSC Ensembl
Innerchr6:162373381..162438043hg38UCSC Ensembl
Outerchr6:162373367..162438057hg38UCSC Ensembl
chr6:162794406..162859082hg19UCSC Ensembl
Innerchr6:162794413..162859075hg19UCSC Ensembl
Outerchr6:162794399..162859089hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3864677
hg1964677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12621254, essv12621257, essv12621260, essv12621255, essv12621259, essv12621258, essv12621256
SamplesHG02272, HG01051, NA19076, NA21135, HG01323, HG02182, HG00593
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611528
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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