A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661906



Internal ID2894993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162337895..162340111hg38UCSC Ensembl
Outerchr6:162337738..162340264hg38UCSC Ensembl
Innerchr6:162758927..162761143hg19UCSC Ensembl
Outerchr6:162758770..162761296hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg382527
hg192527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5903857, essv6071183, essv6025392
SamplesNA18535, HG00475, HG00542
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661906
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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