A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611477



Internal ID6651695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161815923..161848932hg38UCSC Ensembl
Innerchr6:161815960..161848896hg38UCSC Ensembl
Outerchr6:161815887..161848969hg38UCSC Ensembl
chr6:162236955..162269964hg19UCSC Ensembl
Innerchr6:162236992..162269928hg19UCSC Ensembl
Outerchr6:162236919..162270001hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3833010
hg1933010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1232e214
Supporting Variantsessv12619503
SamplesNA20754
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611477
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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