A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6012733



Internal ID8990136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162162737..162165776hg38UCSC Ensembl
chr6:162583769..162586808hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg383040
hg193040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665113
Supporting Variants
SamplesNA19438
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6012733
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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