A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610841



Internal ID6651067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132744922..132750380hg38UCSC Ensembl
chr6:133066061..133071519hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg385459
hg195459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12554755, essv12554754, essv12554756
SamplesHG03484, NA19172, HG03123
Known GenesVNN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610841
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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