A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677740



Internal ID4722074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129282181..129283320hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6026936, essv6076060
SamplesHG00463, HG00557
Known GenesLAMA2
Method
Analysis
Platform
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677740
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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