A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664853



Internal ID9584272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:83173477..83173966hg38UCSC Ensembl
Outerchr6:83173440..83174016hg38UCSC Ensembl
Innerchr6:83883196..83883685hg19UCSC Ensembl
Outerchr6:83883159..83883735hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6122380, essv6488160
SamplesNA19908, NA19257
Known GenesPGM3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664853
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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