A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6025392



Internal ID9002795
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 StatusS
Merged Variantsesv2661906
Supporting Variants
SamplesNA18535
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6025392
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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