A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669542



Internal ID9935647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162162534..162165890hg38UCSC Ensembl
Outerchr6:162162163..162166260hg38UCSC Ensembl
Innerchr6:162583566..162586922hg19UCSC Ensembl
Outerchr6:162583195..162587292hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg384098
hg194098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1167e199
Supporting Variantsessv6589118, essv6570749, essv5607151, essv5817543, essv5458601, essv6493955, essv5951920, essv5498903, essv5862024
SamplesNA19648, NA19678, NA19771, NA19782, NA19720, NA19749, NA19747, NA19661, NA19755
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669542
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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